Tag | Content |
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EnhancerAtlas ID | HS091-25039 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:10282500-10284580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr2:10283366-10283381 | TGGACTTTGTCCCCA | - | 6.34 | Hnf4a | MA0114.3 | chr2:10283364-10283380 | CCTGGACTTTGTCCCC | - | 6.77 | ZNF263 | MA0528.1 | chr2:10284111-10284132 | CCTTCCTCCTCTCCCGTCTCC | - | 6.42 | ZNF263 | MA0528.1 | chr2:10284114-10284135 | TCCTCCTCTCCCGTCTCCACC | - | 6.5 | ZNF263 | MA0528.1 | chr2:10284105-10284126 | TCTTCCCCTTCCTCCTCTCCC | - | 6.71 | ZNF263 | MA0528.1 | chr2:10284102-10284123 | CTTTCTTCCCCTTCCTCCTCT | - | 7.99 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I010143 | chr2 | 10284028 | 10285287 |
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Enhancer Sequence | AGGTGAGAAA TGATGGCAAC TCGCACGGTG GGGGAAGAGG GGCCACTGTG GAGGTGGCTT 60 GCGGGGCCTG TCATCTGCTG TTTCCTAGCT CAGTGTACAG GGCCCCCACG CACCCCTGCC 120 AGGTCGGAAA TCCAGGTACT GCCAGCCTCT GCCGTTCTAC GTGTGGCCAG GCGGGGGAGC 180 TTCGCCCTCC CATGTCCCTC ACCCCATGCC CCAGACAGCA CGGTCCTGCG ATCCCCCTCC 240 CATTCCAGTG CTCAGTATAG CCGTATCCCT GCAGGCTCAG GCCCCCACCA TGGCCAGATC 300 CCCCACCCCA CCTTCACCCT CCGCCAGTCC ATTGCACACA TAGCATCTGG AATGGTCTCG 360 GGCAGCACCT CAGACGATGT GGCTGTGTTG CATGAGCCCC TCCCCTCACC GCAGCTCTCG 420 GCCCTGCCTG AGCCCAGGTG CCCGCGGGCT CCCCGCTCAC CTCTGCCTTG AACCTTCCTG 480 AGTCTGAGCT TCTTTTTTGT TTTGTTTTGT TTGGTTTTGA GACAGAGTCT TGCTCTGTCA 540 CCCAGGCTGC AGTGCAGTGG CGCGATCTCG ACTCACTACA AGCTCTGCCT CCTGGGTTCA 600 TGCCGTTCTC CGGCCTCAGC CTCCCGTGTA GCTGGGACTA CAGGCGCCCA CCACCTCGCC 660 TGGCTAATTT TTTGTATTTT TAGTAGAGAC AGAGTTTCAC CGTGTTAGCC AGGATGGTCT 720 TGATCTCCTG ACCTCGTGAT CTGCCTGCCT TGGCCTCCCA AAGGGCCGGG ATTACAGGCG 780 TGAGCCACCA TGCCTGGCCT GAGCCTGAGC TTCTTAAACA CCACATCCTC TAGCCTCCTG 840 CCTTCACACA GGCTGTTCCC TTAGCCTGGA CTTTGTCCCC ACCCACCCGC TCCTGATCTT 900 TCAGGTCTCA ACTTACAGGT CACTTTCCCT GGGAACCTCC TCAGACCCAG TGAGGCCAGA 960 TTAGGGGCCT CCTCAGAGCC CTCATGGCCC CAAGTGTTTA CCACTTCGCT TTTTCATACT 1020 ATCCAAAGTG CACAGAATCG TACACTTTTC TGATGCCTTG TTCCAGCTGA GTGCCCTGAG 1080 GGCAGGGATG GGGTCCGTGT CCTCCGGTGT GCTCAGCCAG CACCTGGCCA GGCACTCTCA 1140 GTGTTGTTGA ATGAATGAGC GAGTGAGTGA CCCGCAGGGG AAGCTGCTGT GTCTGACACG 1200 GTAACGTGCA GGTTGCACTG GGGGGGCCTG GTTGAGATCA TGACTGGAGT CCCTGGCCCC 1260 CAGAGTGGGA GTCATCAGTG GGGCTCGCTA CCTCTGCACA ATTTTTTTTT TTCTTTGAGA 1320 CGGAGTCTTG CTCTGTCGCC AGGTGGTACA GTGGTACGAT CTTGGCTCAC TGCAACCTCC 1380 GCCTCCTGGG TTCAAGCAAT TCTCCTGCCT CAGCCTCTCG AGTAGCTGGG ACTACAGGTG 1440 TGCACCACCG TGTCCAGCTA ATTTTTGTAT TTGTAGTAGA GACGGGGTTT CACCATGTTG 1500 GCCAGGATGG TCTCGATCCC TTGATCTTGT GATCCGCCCG CCTTGGCCTC CCAAAGTGCT 1560 GGGATTACAG GCGTGAGCCA CCACACCCGG CCCCTCTGCC CACTTTCTTC CCCTTCCTCC 1620 TCTCCCGTCT CCACCAAGGC TGTCTCTGGA GTGGCTGTGG ATCTGACAGA ATGCATGTCC 1680 GCTCTGCCAT CACTATTCAC GCACAGCGCC TGTTGGGGAC TCTCCTGTAA CCCAAGGGGG 1740 TAGCGGAAGG ATGGAGCTTC AGGCCTTGAG GGCCAGGAAA TGAATGTGGA AGACTGAATC 1800 CTCAGGGGAC CCCAACTCTG GGCCGGGTCT GGGGCTCTGT TTTGAGGACG GGGAGTGGGA 1860 GGAGGTGGCA GCAGGAGCCG GCGTCTGAGG CATCTCCTCA CACTCTTCCA AGGTCAGAGA 1920 CGAGGTCTCA GATACGCTTG CTAATGCACG ATTTATTTCT TTTTCAATTT CCTTTGGAAC 1980 CTGTGCTGTG CAGATGTTCA CATGATGTGG TGGGGAAGTG AGTTTTATAA AACTCTTGGC 2040 AGAGTACCAT TCGGCATCCC TGTGGTTCTA GAGATTTCTG 2080
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