About Enhancer

Enhancer ID: E_01_0937
Species: human
Position : chr5:143275121-143277121
Biosample name:
Experiment class : High+Lowthroughput
Enhancer type: Enhancer
Disease: --
Pubmed ID:  32673938
Enhancer experiment: PCR
Enhancer experiment description: DNA methylation standards (100 %; 75 %; 50 %; 25 % and 0 %) and DNA of a female and male donor were bisulfite treated in three independent trials and were used to generate sequencing libraries for 42 CpGs from the NR3C1 1 F promoter region, 84 CpGs of the SLC6A4 5? regulatory region, 5 CpGs located in FKBP5 intron 7, andadditional 12 CpGs located in a potential enhancer element in intron 3 of the OXTR.

About Target gene

Target gene : FKBP5
Strong evidence: qRT-PCR,qPCR,ChIP,3C
Less strong evidence: RNA-Seq
Target gene experiment description: DNA methylation standards (100 %; 75 %; 50 %; 25 % and 0 %) and DNA of a female and male donor were bisulfite treated in three independent trials and were used to generate sequencing libraries for 42 CpGs from the NR3C1 1 F promoter region, 84 CpGs of the SLC6A4 5? regulatory region, 5 CpGs located in FKBP5 intron 7, andadditional 12 CpGs located in a potential enhancer element in intron 3 of the OXTR.;DNA methylation standards (100 %; 75 %; 50 %; 25 % and 0 %) and DNA of a female and male donor were bisulfite treated in three independent trials and were used to generate sequencing libraries for 42 CpGs from the NR3C1 1 F promoter region, 84 CpGs of the SLC6A4 5? regulatory region, 5 CpGs located in FKBP5 intron 7, andadditional 12 CpGs located in a potential enhancer element in intron 3 of the OXTR.

About TF

TF name : NR3C1(GCCR,GCR,GCRST,GR,GRL)
TF experiment: PCR
TF experiment description: DNA methylation standards (100 %; 75 %; 50 %; 25 % and 0 %) and DNA of a female and male donor were bisulfite treated in three independent trials and were used to generate sequencing libraries for 42 CpGs from the NR3C1 1 F promoter region, 84 CpGs of the SLC6A4 5? regulatory region, 5 CpGs located in FKBP5 intron 7, andadditional 12 CpGs located in a potential enhancer element in intron 3 of the OXTR.;DNA methylation standards (100 %; 75 %; 50 %; 25 % and 0 %) and DNA of a female and male donor were bisulfite treated in three independent trials and were used to generate sequencing libraries for 42 CpGs from the NR3C1 1 F promoter region, 84 CpGs of the SLC6A4 5? regulatory region, 5 CpGs located in FKBP5 intron 7, andadditional 12 CpGs located in a potential enhancer element in intron 3 of the OXTR.

About Function

Enhancer function : DNA methylation standards (100 %; 75 %; 50 %; 25 % and 0 %) and DNA of a female and male donor were bisulfite treated in three independent trials and were used to generate sequencing libraries for 42 CpGs from the NR3C1 1 F promoter region, 84 CpGs of the SLC6A4 5? regulatory region, 5 CpGs located in FKBP5 intron 7, andadditional 12 CpGs located in a potential enhancer element in intron 3 of the OXTR.
Enhancer function experiment: Immunohistochemical staining
Enhancer function
experiment description:
DNA methylation standards (100 %; 75 %; 50 %; 25 % and 0 %) and DNA of a female and male donor were bisulfite treated in three independent trials and were used to generate sequencing libraries for 42 CpGs from the NR3C1 1 F promoter region, 84 CpGs of the SLC6A4 5? regulatory region, 5 CpGs located in FKBP5 intron 7, andadditional 12 CpGs located in a potential enhancer element in intron 3 of the OXTR.

About SNP


Enhancer associated network

The number on yellow line represents the distance between enhancer and target gene

Expression of target genes for the enhancer


Enhancer associated SNPs