Tag | Content |
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EnhancerAtlas ID | HS091-15478 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr15:79887320-79889550 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr15:79888522-79888541 | CAGCTCCCCCTAGAGGCTG | - | 6.05 |
| | 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 |
GH15I079596 | chr15 | 79888461 | 79888650 |
| Enhancer Sequence | ATGAGATCAG CTTGGGATTT CTTAAATGTG CATACAGTAA AACTGTAATC TTTGTTTAAA 60 AAAAAGCAAA ATAAATTCTT ATTATCCCCC AATATTAATA CTAACATTAA GGTTTCTCTA 120 ATGGTATTCC ATAATATTAT CTTTTATACA GAAACCCAAA GTCGGCATCT AAAATGTTTA 180 TTTAAAAAAT TGAAAATGTT AAGACCTGTA GCAAGCACAT TATCATTAGA TTTTCTGACA 240 TTTTGATTAA TAAAATATCA CCAGTCTGCT CAGATACATA CTATAAATCA TCTTCCAGAC 300 ACCTGGACAG GCAGCATCCC TGACAGCTGT TCCCACAGCC AGGAGTGGTG TCAGAGTTGG 360 TGGGTGCCTC ACCTCGGAAG CTATGACACA TATAAACACA TTGAAAAATG CAATAATTAG 420 AAGCAGTGCA GTCAGGTTGC AAAATGGCAG GACGAGGGGT CTCCTTGAAG GCCCCTCTGT 480 GCTTCCCAGG AGGAGTCAAG TGCATTCGGC GACATTTGAG GTGACACCGG CCAGGTCGAG 540 AATTGCACAG ATGGCTTCCC AGACTGTGTG CTTCCTTTTC TCCACTGCAG CCTCCAGGGG 600 AGGATTGATT ACTTTGTTCA AAAGGCAGAA TCAGCAGATG TTATTGATAT GGAACTCTAT 660 GGGACTGGAA TTCTGTACTA TGGATAGCAC ATGAGGCTTT TTTTTTTTTT TTTAAGCCAA 720 AGCAGCATTA GTGGAGGCTT TAAAAATAAG CCACAGTTCC CGTTTTAATG GATTCAGTGT 780 TAGGTCATGT GCACAATCTG TTATTTAAAA TGTGCATTTA CAGGCCGCTG TTGAAAATAC 840 CTGCTTTTAA AATGCCTTGG GCTTCAGACT TGCTACGTAG GGCAAGACTC TGTCACAAGA 900 GTTGTCTCTT TCATCAGCGT CTGTCTTTCC TGCTCAACTG GAGACACTGA ACTCCCTACC 960 ACAGACATCT TTTCTGGGAC AAGTATATTT GTCTCCTTTT TGTCTCTGAT GATGAAGGAG 1020 AAAGAGTGTA AGAATATGAG ACACTGGCCA ATGACAGTAA AACGATCTAA AAAGAAATAA 1080 GCCAAGAAAT TACAGTTTAA ACCTCTTTCT TGTGCACACT CTGCCTCCTA AGAGTGCGAT 1140 CCAATCACAT GACCTCTCTG CCCCATCAGC TTTACTCCCC CGGTCCACCC TGTGAGGTTC 1200 TTCAGCTCCC CCTAGAGGCT GGAGTATGTT ATGAGCAGGA ACCACAGCTT CACCTGTGGG 1260 TAGGAGCCCA TGGTCCACCC TGTGAGGTTC TTGAGCTCCT CCTAGAGGCT GGAGTATGTT 1320 ATGATCAGGA ACCACAGCTT CACCTAGACT TCTGTGGCCA AAGATTTAGT ATCCAGGAAG 1380 AGCATCAGAC ACTCCTATGT CCATCGGGTC AGAGTCTTTC CTTGACCTTC TCCTTCTTTT 1440 CTGCATCCAA CAAAGTTGAT GCTTCAATTC TCTTTCCTGG CATTCTTGGC TCATATCTGT 1500 TAGGCTGGGT ATGGGGGAAA GATGCTAGAC CCTGAGTCCA GTAGTTCCAA CAGCTAGGTC 1560 CTGCTCTGAG TTGCTCACTC ACTCAGAAAC AAAATTTTCA TGATCAAACT GCACCTTCTG 1620 TCCTTATGCC CCACTCATCA GAGCAGCCCT CCGGTGCCAG CCAGAACTAA GTCTAAATCA 1680 AGCCCTAATT ATTATCTAAT AAGCCTTGAT CTCCCTCCCA GGGTCCCTTG CAGTAGGCAC 1740 CATACTCCCA GGCCACAGTC CTGCCTGACC CCCACTCATC ATCCCTTTCT ATTGTTAGCT 1800 TTGGCTGCTG AGGTATCCAT CCACCCAGGT GTCAAGATGA CCAAAGACCC TCATTCAACA 1860 GATACTCACT CAACCCCTAC CACAAGCCAG GACCTGTGCC CAGCATCCAG TCCCCAAAAG 1920 GAACATGATT CCTAGCCCCC ACAAGCTCAC AGTCTGGTAC AGGTGAGGCA CCGGTGAGTA 1980 TTTTCTGTGA AGGGAGTTAA GTGCCAGCTC TGTTAGAGGG TAGCAGGAGG TCCTATGGGA 2040 GTATCACTGG AGGCTGACCA GCAGGACTGG GTTTCCCAAG AGGCAGACTG GGCAGACAGG 2100 CAAGGCAAGA ACATAAAAGA ATGGAGGAAA AAAATAAAAG AATATCGATC TATCCAAAAA 2160 GAAGCCTTGA ATTATCATTA TGGGAAAATC AGAATTTTTT GGACATTCTT ACATAGATTT 2220 CATGGTTCGG 2230
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