| Tag | Content |
|---|
EnhancerAtlas ID | HS053-03214 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:185410000-185411300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr1:185411040-185411056 | ATTTCCTAGAGAGCAA | - | 6.65 | | BCL6B | MA0731.1 | chr1:185411038-185411055 | GTATTTCCTAGAGAGCA | - | 6.61 | | IRF1 | MA0050.2 | chr1:185410037-185410058 | AAAAAAAAAAAAAAAGTAAAT | - | 6 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I185438 | chr1 | 185408004 | 185412576 |
|
Enhancer Sequence | CCAGCCTGAC TGCAGAGTGA GACTCCACCT CAAAAAAAAA AAAAAAAAAA AAGTAAATGT 60
AGAATTTGTT CTAATACTCA AGGGATGAAA AATTTCTCCA AGCTAATGAT TGTCTAAAGC 120
ACATATTTCT ACTGGGACAT GTTTTAATTA CTGGGCTGTG GAAATCATAT GACATGGGTT 180
GGAATGTGAG TTGTTCTGTC TGTTAAGTGA AGAATTTTTA GTGGCTGCAT TTTTTTGAAT 240
GAAACATTGA GTCACATGAT CTGACAAGAA AGAATGTACT TATGGGGTCA ATGGGACAGA 300
ATACTGGACA TTGGAAAATT TCCAATAGGA ATAGGAAAAC ACCAGTTTAT GTTATATAAC 360
ACCACCATCA CTATTACCAC TACCACTGCC ATCACCTACA AAAATAGGAG CAAAAGCCTT 420
CTAAGCACTG TGTCAGTGTC TGTTCTGCAT ATTTTATGTC TTGCATTAGT CAAGGTTCAA 480
CCAGAGACAC AAGACCAGCA GGACATATAT AAAGACATTT ATTGAGAGGA ATTGGCTTAT 540
GTGATTGTGG GGGCTCTGTA GGTGAGGCTG TTAGGAAGGG CAGGCTGGAA CCCTGGGGCA 600
CGAGCTGAGG CTACCAGCCA CAGACAGAAT GTCTTCTTCC TCTGGGAAAC TGCAATTTGG 660
TTTTTAAGGT CTTTCGCTGA TTGAATCAGA CCCACTCAGA TTATTGAGGA TAACCTCCCT 720
TACTTATAGT CAGGTTTATG TACTTTAAGC ACATCTACAA AATACTCTCG CAGGAGCACT 780
GTGATTAATG TTTGGTTGAA TAACTGGAGA CTGTAGCCTT GCCAAATTGA CACATAAAAC 840
ATGTGTTATC TCATTGAATC CTCAAAGCAA CCTCTGTGAA GCAATTCACA AGAATGATGA 900
GTGTTGGAGC AGGGGTTTGA ACCTAGGTGA TCTGATATGG AACCCAGGGA TTGTGCACGA 960
CGCTGGAATG CACCATGGGC AAGAAGCCAA AGCCACACAT AAGTTCTCCT CTGAAACATC 1020
TCCTGGAACA GGCCCTTTGT ATTTCCTAGA GAGCAATAAG TCCCTTATAA CTAGGATTGG 1080
TGGCTGTTCT CAGGCTGTCA TGTGGAGGAT ATTAGCTAGC ATCCTAGTTA TAGTAAAAAG 1140
AACTTAAAAT CATAAGTCCC TCGAAAAATT GCTAAGTCTC CTTAGTTTCA TTCAAAGGGT 1200
ATAAAGAAAA CATGCAGTTT GTCATCCCAT TCACTCCTGT CACCCCCAAG ACATTGTACT 1260
AAGACCATAA ATAGAAAAAT TGGTATTGAG ACAAGCATTG 1300
|
