| Tag | Content |
|---|
EnhancerAtlas ID | HS091-46763 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr8:125978200-125980530 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr8:125980281-125980291 | CTCAAGTGGT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATACTTCCTT CCGAGAATTT CTGGTCTAAC CAGTTGTCTA GCTTCACGTC CTGTTTCTAT 60
GGATTGTTTG TAACCAGCTT TTGCTGCAAC TGTTACTCTG ATTAATATCT TGCTAATCAT 120
AGGTTATGGA AAGACTGTGT TTCTGTTTTA AGGCTCTGTT AGAAATTACT GATGCACACA 180
CTATATTGTA AATTCTTATC CCTGTATACT GTACTTCTGC ATACAGATGT TATGTTAAAG 240
AATTACTTCA TCTCCATGTG ACCATCACAC CTCATAATCA AATGACCCTA AATCCCTCAC 300
TAACCTACCC CCGCCCTCAC TAAACTTAGT AATAAATGCT GGTATATCCA GTGCATTGTT 360
GGCATAGCGG GACCAGAAGG CAGTGACCCC CCTGGACCCA GCTTTCACTA TCGTGTGTGT 420
CTATTATTTC TCTACCTGCC GATCTGCCTG GGAACAAAGA GAGAGCCCCG TTGCATTGTG 480
GGCTGCTGGC CAGATCCCGC AATAAATAAC CTCCTAAAGT GTAACTCAAA TATATAAGGA 540
ACATGAATAC TTATAATGTT AGAATATAAA ATGCTTAAAT TTTGCTTTGT GATCACCAAA 600
CAATATGGTT GTTAAGAAAA AGCTGCTTAG TTGGCAGTAA CATGGCCTTT CTCATGCTCA 660
TCCTAAAACA TCCTAAAACA TGGGGCAATT TTTTTTTTTT TTTTAGGCAG GATCTTGCTC 720
TGTCACCTGG GCTGGAGTGT AGTGTGGTGT GATCATAGCT CACTGCAGCC TTGAACTCCT 780
GGGCTCTGGT GATCCTCCCA CCTCAGCCTC CTGAGTAGCT GGGACTACAG GTGTGTGCCA 840
CCATGCCTGG CTAATTTTTT TATTTTAAAT TTTTTGTTTT GTAAGTTGCC AGGCTGGTCC 900
CGGACGCCTG GGCTCAAGTG ATCCTCTCAC CTCGGCCTCC CAAAGTGCTG GGATTACAGG 960
CGTGAGCCAC CTCACCCAGC TTCAACATGG GCATCTTGTT TGCTGGCATA CGACATGCTC 1020
TTCATAATAT CTACAGCAGT GCTTCTCAAC CCTCTTTTCC TTATCATCCC CCACCCCATC 1080
TTTTCAGACA TTTTTTATTA ACCACTCCCC CTCCATTAAA ATGTAACACC ACAAATACAC 1140
TGTATAACTG TTTAAGTCTT CTATGATGTA TGTCTGTGCT TTATGCATGA AAAGGGTATT 1200
TTTTTTTCAT GCTCCCCCTG AAGAACTCTT TTGTCCCCTT GGGGGCGATA TCACCACTGT 1260
TGAGAATCGG ACCCCCTTCC TCCATCTTCC AATAACAGTT TGCTCATGGC TAGAACAGAT 1320
AATTAGAAGG CAAGCGTCAC TCTTCTTTCA TTTCCGAGCT GGACCTGTGG TGCCAGGCTC 1380
AGCCTGCTTA CACACACCAT ATAGCCATCC TCCAGCTGGA AGTTCTGTTT GAAAGCTTGC 1440
TACTCCAGGG AACGCACAAA CTTTGTCCGT GTGCCCTCAA CCCCAAACTA GAGCCTCCCC 1500
AGCAGTTTAG CTGTGTACTA ACTAGAGTCA GTTACAGAGA ATAGAATTCA CTTGAGCTGA 1560
CATAAGGAAT AATAGATATA TTACAAGGAT TAAAGGACTT TTGGAATCTC TGGGAGGACT 1620
GAGGAAATGG ACTGTGGGCT GAGCTTCCAG GAGTGTCAAT CAAAGGTGCT GCTACAACTA 1680
TGGCAATTAC AGCTTCAAAG AAGTCTTGGA AATGTAATGT TTAGCTTTTT CAACTGTATT 1740
AGTCTGTTTA GGCTATCATA GCAAAATACT AGACTGAGTG GCTTAAACAG CAGAAATTCA 1800
TTTTCTCACA GTTCTGGGGT TTTTTGGTTT TTGCTTCTTT TGTTTTGTTT TGTTTTTTGA 1860
CAGGGTCTCA CTGTGTCATC CAGGCTGAAG TGCAGTAGTG CAATCATGGT TCACTGGAGC 1920
CTTGAACTCC TGGGCTCAAG CAATCCTCCC GCCTCAGCCT CCTGAGTAGC TGGGACTATA 1980
GGCATGTGCC ACCAATGCAA AGCTTTTTTT TTCTTTTTTT TTAAAAATTG TTTGTACAGA 2040
TGGAGTCTCA CTGTTGTCCA GACTGGTCTC AAACTCCTTG GCTCAAGTGG TCCTCGTGTC 2100
TCAGAGGTAC TGGGATTACA GGTGTAAGTC ACCATGCATG GCCTCATTTT CGCACACTTC 2160
TGGAAGGTAG AAGTCCATGA TCAAGGTACT GTCAGTGTTA GTTTCCATGA GGCCTGTCTT 2220
CCTGGTTTGC AGATGGCCAC CTTCTTGCTA TGTTCTCCCC TGGCCTTTCC TTTGTGTGTA 2280
CACAGACAGA GATGTCTCCG GTGTCTCTTC CTCTTCTTAC AAGGACCCCA 2330
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