| Tag | Content |
|---|
EnhancerAtlas ID | HS113-25033 | Organism | Homo sapiens | Tissue/cell | Keratinocyte | Coordinate | chr3:58207030-58208480 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr3:58207951-58207962 | AGTGACTCATG | + | 6.14 |
| | | 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 |
| GH03I058221 | chr3 | 58207482 | 58208734 |
| Enhancer Sequence | TGCTCATAGC TCACTGCAGC CTTCACTCCC TGGGCTCAAG CGAGCCTCCC GCCTCAGCCT 60
CTCTAGTAGC AGGGAGTACA AGCATGCATC ACCATGCCTG ACTAATTTTT GTATTTTTTG 120
TAGAGGCAGT GTTTTGCCAT GTTGCCTAGG CTGGTCTCAA ACTCCTGGGC TCAAGCGATC 180
CTCCCTCCTT GGCCTCCCAA AGGTGTGAGC CACTGTGTCT AGCCAACATA ACTTTTATAT 240
GCACTCAGAA ACCAAAAACC TTGTGATACT CACTTTATTG CAGTGGTATG GAGCTGAGGC 300
TGCAATATCT CCAAGGTGTG TCTGTAACAG TGGCTGTGGG TTCTGACCTG TGGTAGACCC 360
ATATTACACA TCTTTACATG GACTCGGTCC TTTAAACCTC ACAACTACCT GACTACTATT 420
ATTCTCTTCA TTTTACTGAT GAGGAAACTG AGCTTCAGAG AGGGCAAGTC ACCTCTCCAG 480
GTCTCACATC ACATCTGGTA AGAGGCGTGG CCAGGACTGT TTGACACCAG AGTGTGACCA 540
CCTGGTCAGT CTCCTATAGC ATTTCTTCTC TGGCACATAA CAGTGACAAG GCCCTGCCAC 600
TATTCCAGCT CAGAACACTG AGAACAATCC ATGTCCCTGA CCCCAGATTC CCAGCAAATG 660
GAAATGCTTT CTCTCCATAT TCTGAAAGCT TCTGTGTGTC CCATACATAC ATAAGGAGCC 720
TGAGGGCTTG GGGGACACCC TGGCTGTGAG CAGAGGGCCC CAGAAAATCA TCTGTTGTTC 780
TTTGGGAGAA GGCTTCCCTC CTGAATCATC ATGCATTAGG CATGATCTAT AAATTTATCT 840
ATAAATCTAT CTAAAACCAC ACCAGTTCTA AAGACAAGGT TTGCAGTGCA GGTAGGAGCA 900
CGTGTAAATC CTTAACTACA CAGTGACTCA TGAATGATTT TCCAGGCAGG AATTGTTGGG 960
AGCCAAAAAG GCCAAAGGGA TTGTGACCAG CTCAGCATTC CACTGGACGC TATATGATCA 1020
AACAGCAAAC TGTTTATCAT GAATGCAGGA TGTGAGCAAA CTCACACTGC ACCTGCCACT 1080
GAAAGGTTTG CTGAGGGCCA ACACTCCCTG GGGGCCGGGC TCCTTGAAGT TATCTACTGA 1140
AAAATCTAGC ACCTATCATA CAAAGGATGC AGTCTTGCAA GCCTGCTGTG AACCAAATGG 1200
CCGACTGACA ATTACCCAAC AACCACCACC CCCTTTTCTC GTTATCTCTT TTACCAATAA 1260
ATACGGAAGG CTGTGTAAAG CTCAGGGCCC TTGTCTACTA GAGGCAAGGT GTCCCTGACC 1320
CCTTCTTCCA AATATACTCT TATGTCTTTG TCTTTTATTT CCGCATTCCC CCTCTTTGTT 1380
CAGTCCACCA GGTCCGTGCA GGCTACAAGG AATCCCATTC CCAGGAAGGG ATCTCCCCCT 1440
CCAGGGGCAG 1450
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