Tag | Content |
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EnhancerAtlas ID | HS118-18929 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr9:2426550-2428270 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr9:2428193-2428205 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr9:2428197-2428209 | AAACAAACAAAC | - | 6.32 | SP2 | MA0516.2 | chr9:2427840-2427857 | ACAACCCCCGCCCCCCG | + | 6.34 |
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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 |
GH09I002426 | chr9 | 2426439 | 2428200 |
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Enhancer Sequence | CTCAAGAATC CTAATGAACC TCTCCAGCAC ATTTCTCTGT GTACTGGAGA ACCAGTGATG 60 AACACTATTC TTGAAACATC GCTAGAATTG TCCATACTTC TTTTCTGTAT GACACCTCTT 120 TTCATTTGGT TGTTTTCTTT TAAATTTTAT TTTGCTAAAA TTCATAGTGA GGTAGGTTTA 180 CATTCTCACA AAATATAATA CAGGCAATCA AGAGATAGTC TAGGAGCCTC TCTTAAGGCT 240 CCTATTACAC ACAGCCCCCA AGTACTGGGA CCCCTTCAGA CCATCTCATT TTTAGGAGGT 300 GTTCCCAATC ACTAACAATG GCCTGTGTCA AAATGCCTCC CCATAGTGAT AGCCAACGTC 360 CTGAGCAGGT GTCTATGTCT CAGGCAGCTG GTCTCTGTAA GGGGTATCCA ATTATGATGA 420 GGCTCCAGGA AGACGTATAT GGGTGTAATG AGAAGGATGA CGGAATGGGA CCCAGGAGAC 480 ACCCCACAAC CACTATCACC AAAGCCTGGA CATTTGTTCC TGCCCATTTC TATGCCCATA 540 TTTCCTCCTT TGCAAAATAA ATAGTTCAGA CTAGAAGAGG CCTCAGGTGC TATCGAGCTT 600 AGACGATTTA TGACCTTCTG AGTACTGTAA GTGTTACCTG CTTTGGCAGT TTGCACTAAG 660 AATCGGACTT TAGAGATTTG GCACACTCTG ATGTTTGTTC AGTTGGTAAG TGTGCTCAGT 720 TTTTGTGGCA TGTGTCTACA AAGCACAAAA GCCTTGGTTT CTCTGGACTT CTGAAGTGCA 780 AGAGATTGAT AGCAATCCCA GCCCATTCCC AGGGAGAGAC GCAGAAACAA CTCTGTGAAA 840 GGTTACTTTG GTCTCTATGG GAACCACTCT GTGCCCTTGA CAGAGAAGAC AGCTTGGGGA 900 AGGGAGGCAC ATCCGAGAGC TCTGAAGCCT GGGCAGAATG CCCCATGGGC CCACAATGCC 960 ACATACCTGT GAATGGAGAG AAGGGAACAG GCAGTCCCAG TGTGCATATT TGGAATCCAA 1020 AGTCCTATTT GACCTTAGAT ATTTGGAAGT AGGTGGGACC TGGAAATGCT AACACCCAGA 1080 GGCCGTGCAG TGTAGTGGAA AGAGAACTGG CTTTGGAATC AGAGGTTCTG GTTTGACTCT 1140 CAGCTCTGCC CTTACTAGCT ACGTGACTTG GAGAAGGTCT CCTAACCCTG CTGAGTGTGG 1200 GTTTTCTTGT CTGTCCAGTG AGAAGCATTA GGTCTTTCCT GATGATCTCA TAGGGCTGAT 1260 GTTTCTGGTT ACTTTTCCTG CACACAGTGT ACAACCCCCG CCCCCCGTGA TGCGTCAGTC 1320 ACAGTCTAAC AACAATATTA AGGAAGGATA ATGATAAAGT TAATTTTTGT GGAGAATATA 1380 ACATTGATGA TATTGCTACC CACTGTTGCA TTCTTAATAT GTACTAGGCA CTCTGATAAG 1440 GACTTCAGAA ACATTAATTC ATCACCTGAG ATCACATGGT TGGTAAATCA CATGGCAGAA 1500 CTAAACTCAG ACGCTCTGAC TCCAGAGCCA AGGTCTTAAC CCAGTGCGTG GTTCATCCCT 1560 CCTAAGCCAA CAACCAGATT TCTTCCAGTC CTGGCTTGTA GAGAGTGAGA AAGATGTGCT 1620 GGCTTGTCTA CTCACATATT AACAAACAAA CAAACAAACA AATAATTAAG CAAATCAGTC 1680 AAATCCTTTA AAAGAGTCAA ACACAGCAAC TTTGGAAAAT 1720
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