| Tag | Content |
|---|
EnhancerAtlas ID | HS053-03197 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr1:184604310-184605700 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr1:184605449-184605460 | CTTCCCAGAAG | - | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH01I184636 | chr1 | 184604508 | 184604715 | | GH01I184635 | chr1 | 184605121 | 184605270 |
| Enhancer Sequence | AGCCTTCCTT TGTTCAACCA AAACATCTTT CCTAAATTTG TCCCTCCTGG ACCAAATCTG 60
ACCAACAACC TCTCACTAGT GGAAAAGCAC TGCCGAGAGT GTGAGCTGAA GCAGCCAGTC 120
CCTGCCCCCC GCCAGCCTGG ACCCAGGCAG ACCGTCCTCC CAGCAGCTAC CATGTGGAGA 180
TCCTTCCTCC TTCTTCTTTC TCCCACACTG CCTTCTCAAG CTTTCTGCTA TTTTCTGGAG 240
CTTTTCTAGT CGTCACCCAG ATGACCTGGA GATAGTCCCT ATTGGTCATG AGTTCTGCCC 300
TTTTCTCTCC AAGCCACTCC AGAGAGACCT GTTCCCGTGA GTCACTGTGG CATCCTGGCC 360
CATCAGCCCA GGGCTTCCCA CAGCTCTCAG CAGCCTTCTG CTTTGTGTCA AAGGAACTTC 420
GTTTGCCAAA GACTTGTTCA TGTGTTGTCA CTGGATTTAT TTACATTTGC TACATGTCCT 480
ATTGGACTGA AGGACAGTGA AGGTGGCATC CCACTACCCA CAAAGCCACC TCTCCCTGCC 540
CCTCCAGAGT GCTCTGTTCA TACCGCTGAT GCTGAGATGG GCAGCCACTG AGCACGCATG 600
ACATGAGTAA CCATTCCGTC CTCTTGGCCT GGGTTTCCTT CCTGGAGCAA AGGGGAGGTG 660
GAAGCAGGCA CTGGTTGGGA AGGTGACTGT CAGATTAACT CTGATGGGTA AAAATCCTCA 720
GTCTCACAGC ATCTGTGAGC AAGGCAACTC AGCCTCCTGT GAACCCCCTA ATTTCCAGGC 780
TGGTGGGTGG TTATTTTTCC TCCAAAGCCC TCAGCCAGCC CTTCCTCTCA CCCAAGGGCT 840
GTGGTTTGGG GCATGTTTTG ACTTGAAACA GTCAGACCCA TGGCGGTATT TGGAGTTGTA 900
AGCCCCTTCT GTGCTAAAAG GAAAACATGA ATGGTCTATT TAGAACCTGC TAACAATTCA 960
CAGTATGAAA AACAGCCAAC AATTCTGCTG CCGAAATGCC GGCTTTCTGA GAGTAGCCCC 1020
AGGGGAGCTG GCTGTGTGGC AATTCTGGCC CCTACTCTGG AAGACCCTGC ACTAGTGGTG 1080
GCAATGATTC CAGAATATCA TGCCTCTGTC CTGGCTTTTT CTCAGCCTCT CCTTAACCTC 1140
TTCCCAGAAG GCTTTCCTCC AGGGGCCTGC GGTGTTCTTG CGCTGTGAGG GAGACCACTT 1200
TTCATAAACC GTATGAACTT TGCTCTGGAC AAATGAGAGA AGGGTGAGTA TTTGGGAGGG 1260
CCTCAGACAG ATTCTCCTGG GCCTGAGTTG TTAGGTTTTC CCTCACCATC ACAAACATAC 1320
ACAGAGTTCA CCTGAGGGAG GAAGCTGGCT TCCTCTCAGG ACAAAATGGC GTCCCTGGAG 1380
CTGTAGATAC 1390
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