| Tag | Content |
|---|
EnhancerAtlas ID | HS118-10131 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr2:86171860-86173450 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr2:86172465-86172481 | ACTGAACTTTGACCTA | - | 6.74 | | Nr2f6 | MA0677.1 | chr2:86172467-86172481 | TGAACTTTGACCTA | - | 6.26 | | RREB1 | MA0073.1 | chr2:86171912-86171932 | CCCCAAAACACCCATCAAAC | + | 6.43 | | Rxra | MA0512.2 | chr2:86172467-86172481 | TGAACTTTGACCTA | - | 6.54 | | STAT3 | MA0144.2 | chr2:86173205-86173216 | CTTCTGGGAAG | + | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGAAAATAT TCATAGCAGC ACTTATTTGT ACTAACCCTA AACAGGTAAC TACCCCAAAA 60
CACCCATCAA ACAGTGGGTT GGATAAATAA TTTGTGGTAA TATTAACACA ATGGAATATT 120
GGATCTGTGA CAATTAAACT CCCTAAGGCA TACCCAGGCC CTAAATCAGC ATCAGCAGGA 180
AACAGAGTGT AAACATTATG CAGCTCCAAG AAGCATAATT TTTATGCCCA CTCAGATGTG 240
ACCATGGGGG AAAAGGGATA GGGAAGAGCC TCAGAGAAGG CAAAGTGATG GTCACAACGG 300
ACAATAGATT AGGATGTTCC TCCCAGAAGG AAGAACCTGG GGCTGCCAGA TGGACTAACC 360
AGGCAGCTTA CCCCACTGCT AGGGCTGGAA GACTCCACTC CTCCTCCCCA ACTAGACTTG 420
GTGACCACTA TGGACCAGTG ATGACTGCAT GCTTCTCATA TTCCCCTTTG CTGAACAAGA 480
GCTATAATTG TGTTAACCTA TTCAGTCATT GTTTATCAGA TGGATTGTCT TTTATTTTAT 540
AAGTCACCAG AACATAAACA GCTACAACTA GACCTGATGG GAAGACCTTT GTATTACCCA 600
AAGATACTGA ACTTTGACCT AGATGTAGTA ACTGGATGGG AATTTCAAGG TTTCTCTTTT 660
GGAGGCTGAA CATGTTCCAA ATGTGGGAAT GGAGTGTAAA ATGGACGTCT GATAGCCAAA 720
AGGTAGACTG TGGTAAAGAT TGCTAGTTGC CTATTCCAAT AGCGCTCGTC CTCCTCTTCC 780
AGTTGTCAGA ACCACAAATT CATTTGGAAT GGTAATTGTC TTAGTCCATT TGTGTTGCTA 840
TAAAAAAGTA CCTGGGGCTG GTCAATTTAT TAAGAAAAGA GGTTTATTTG GCTCATGGTT 900
CTGCAGGCTG TACAAGAAGC ATGGTGCCAG TATCCACTTC TGGTGAGGGT TTCAGGCCAC 960
TTCCATTCAT GGTGGAAGTC AAAGCAAAGC TGGCCTGTGC AGAGATCAGA TGGCAAGAGA 1020
GGAAGCAAGA GAGAGATGGG AAAGGTGCCA GGTTTTTTCA ACAACCAGCT TTTGCAGGAA 1080
TTAATAGAGC CAGAAGTCAC TCATTACCAT GAAGATGACA CCAAGCTATT CATACAGGAT 1140
CTGCCCCCAT GACCCAAACA TCTTCCATTA GGCCCCACCT CCAGCACTGG GGACCAAGTT 1200
TCAACATGAG GTTTGGAGGA TCAAATATCC AAGCTATAGT AGCAATGCAA CCTACTAAAG 1260
TTCTATTATT TCTAGCCTCC CTTTTAGCTA GGTGTGGCCA TGTGACTGCA TTCTGGCATT 1320
GAAGGATAAG CAAAAGTCTT TAAGACTTCT GGGAAGTCTC TTTAGAGAAA AAGGGGCAAG 1380
CCCTCCTTCT CTTGCACATC CTACTGACTG GGATACAGGT GTGAGGGCTG GAGCTCCAGA 1440
AGCCAGCTCA GACCCTGAGA AAGGAAGCCA TTATAGGGCA GTGGAGCAGT GAGCTAGAAG 1500
ACCCTTAACA GTCCAGGATT GTCCAACATC TGACTACTTG CATGCAAGAG AGAAATAATC 1560
TTCTGTCCTT TACAAACCAC CATTACTTTG 1590
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