| Tag | Content |
|---|
EnhancerAtlas ID | HS118-17124 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr7:36989010-36990690 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr7:36989067-36989078 | CCACACCCTCT | + | 6.02 | | Klf1 | MA0493.1 | chr7:36989065-36989076 | GGCCACACCCT | + | 6.32 |
| | | 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 |
| GH07I036949 | chr7 | 36989206 | 36990006 |
| Enhancer Sequence | TCATCTGGTT CCTTTGATGA CAGACCAGCT GAAGAGCCCC CTTCTCAATG TGCATGGCCA 60
CACCCTCTCT CGGTGGCAGA CATCAGACCA GGTTCTCTTG CTCTGTCCTC TTCACTCGGT 120
CTAGGCCAGG GTTCTTCAAC CTTGGCACTA CTGACATTTG GGCCAGATAA TTCTATGTTG 180
TGGAAGCCTG TCCTGTGCAT TACAGAATGT TTAGCAGCAT CTCTGGCCTC TATTCACTAG 240
GTGTCAGTGG CCCCCCACCC CCAACCAAAT GTGACAAAAC TATCTCCAGA CATTGCCAAC 300
TCCCCTCATC CCCATGGCAA ATCCTTCCTG TTCACTGTAG AATGTTTAGC AGCATATCTC 360
TGGCCTCTGC TCACTAGATA CCAGTGCCCT CCTCCACCAC CCCACCCAGA TGTGACAAAC 420
AAAACTATCT CCAGACATTG CGAAATCCCT CCTCCCATTT GAGAACTACT GTGTGGCCTC 480
ATGCCAATGA CACAGACAAT GCAAACATCT TTCCAAAGCA AATCCCCAAA GTCCCGTGGC 540
TAAGCTGGTT CTGCAAAATT AGCTTCTCAG ATTTAGGTTA TGGCTCTTTC GGTTGGAGTT 600
CCCTCGTGCT GTGTTCGCCC CCATGCTCCT ATACATCTCA TTTCCATTCT CCCCTTCTCA 660
CTCACCACTT TTTTTCAGCA TTTAAATCTA GAAGATACAG CTCCCTGTAT ATCCTAAACA 720
GACACAGAAA ACAAGAAACA ATGTACTATG CAAGACCCAC CATCAACAAG GTGCCCGGGA 780
CAGCTGGAGA TGAGCGACTC CTGACTGGGT GGATTGACTG GCATGCTCAT TATTAACATC 840
TGTGAGAGAC AGAGGGAATG TTTCCTTCAG CCCTGTGAGC AAGACTCAGG AACTGAGCAG 900
CCCACAGTAG CTTTTTATGT AACCAGCCCA CCTTCTCTGC AGGAGATGAG CAGAGTCAAA 960
AGATCTGTTT TCCTTCCCAT TTCCTCCTGC AGTTCACTCT TCACAGTGGG TGACTGGGCA 1020
AAGGGTCACT CACCACCAAG CCACAGGTTT CTCCTATTTT CTCCTGGGCC CCTGGCCACT 1080
CCTATCTTCT GCTTCTGTCT TTGGTTCAAC CCCTTGGGCT GTCTGTGTTT CATGGCGCCA 1140
GGCAATTTAT CTCTTTTGTC CTTCCTAAGG TGAAGGTAAC AATTATACAT CTTTAATCAA 1200
GGCTGGGGAC TGACTCAATA TTTTTCTGAC AGGAATACTG CTCTTCCAGC AGACCGAGTC 1260
ATTTAGGTAT TTCTCAAATG TTCACTGCAC ACAAGACATT GCGCTAGAGG GACAGAGCCC 1320
TTATGGAGAT CGAAGCAATG GCTCCTTCAT CTCCATGAGG GCTCAGGGGT CTGGGCTGAA 1380
CTGAGGACTG GCCCATGAAG ACAAGCTGAG GATGCACTCC ATGAAGCTGT TTACAGTGGG 1440
ATTTCAGACC CACCATGTTA CGGAGTGTCT GAGAGGAAGG CCGAGAGGGC GTGTCTGCTT 1500
CTTGCCTCTC TGGAGCAGTA AATGACCCAT CCATCTACCC AGTTACTGAA GCCAGACACC 1560
AGGAAGTCAA TCATGATTCC CCCTCTCCAC CACTACCCCT GTCCACACCT AATCAGTCCA 1620
CAAGTCTTTT TGAGCTTATT TCTAAAACAT ATCTCACAAG TACCTTCTTA CCTTATTCCT 1680
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