Tag | Content |
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EnhancerAtlas ID | HS091-21182 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:73954780-73956290 |
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) |
Gata1 | MA0035.3 | chr17:73955398-73955409 | ACAGATAAGGA | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 73955254 | 73955493 | chr17 | 73955538 | 73955972 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I075958 | chr17 | 73954902 | 73956819 |
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Enhancer Sequence | CGGGAGGCTG AGGCAGGAGA ATGGCGTGAA CCCGGAAGGT GGAGCTTGCA GTGAGCTGAG 60 ATCGCGCCAC TGCACTCCAG CCTGGGCGAC AGAGCACGAC TCCGTCTCAA AAAAAAAAAA 120 AAAAAAAGTA TAAAAGTATA ACTGTTATTG GGGAAATGAC CTGAAATGTG ACTTTTAAAA 180 ATTCCTAAAG GTCCAATAAT AAGGTCTCAG TTGACCCTAG AGATTTCCAA TGGCAGGCCT 240 AACTTAGTCC TGCTGGTTCA TTAATGTGGC AAGGAAGAGT TTCCAGTTTC TTATGTGTAC 300 TGGGATAGAC AGGATCTTAT GTTTTAAATC TTAACACAAA TATATCAAAA TTATTTGAAA 360 AGAGTCATAG AAAAATGTTC TAGGTGGCAG TCTCTACAAA AATACTGTAC TAAAGCAAAC 420 GTTGGGAACC TTTTACCAAT CTGCTTTCAT AACGCTTAGA CCTCATTAAA CACACTTTGA 480 AACATTTAGA AGCTTCCAAG TTGAATAACC AACTTATGTG CAATCCACAA CTTTCCCGAG 540 TGGGAGTCAA CAAATCAGAC ACAGACATCT TTCATCAAAG AAGCAGCTTT TACAGAAAAG 600 CAGATAACAT TAAACAGAAC AGATAAGGAC AAAATGTTTT CAAAAGCACA ACTGAAACAA 660 ATAGTATTCC ACTTGGAGTC TCATGAAAAT CCTGTAAAAT ACTATTCAAC ACCAAATAAA 720 AAGCAGCAGC TGTATAGAAA TAAGGAGCAA GTGGCAAATA CACACTAGAC CAGTTTTTCT 780 GAAACGTCAG AGCAGAAAAA GAGAAGCCAT AAGCAAATGA ATGGCAAACA CGGACCCAAT 840 TCAGAGAAGA TACAAAGAGG AACAGCGGCC ACCTCCAGCC CACCCAGGTG CATGAAGAAA 900 GCAGGTGGGG GGTGGAAAGA TCAATGAAAG GTGGAGATAC AGAGTCTGAA ACCAAATGCC 960 TGCAAGTTCG GCTTATCTTG GTTTTTTCAC TCTCCAGCCA AGTCACTTGC AGAACTACTG 1020 ATTGACTCAA AGTACAAATA ACTCCAAAAT GTCACACACG TCAGTTATAA GCTACTCATT 1080 TCCCTCAAGC AAATCCAAGA GTACACAAAC TATTATTTGT ATTTCTTCTG GAATTTGTAC 1140 TCATTAAGGT ATCAGTAGTA AAGGTAATCA GATAGTAATG AAGAAAAAAA CAGCTTCGGG 1200 TTGTATATGC ACACAGATTC TATACAACCT CAGTAACATT GAAAAACCAC TTGGTAAATA 1260 AGGCCTGATT TGCAATTCTT GACCCTCTGA AGGGGAACTA TGGTATAAAA AGGACAATCA 1320 TTTTATCAGT ATCATGGTCT TTAATTCCCA CTCACCAAAG CAGTGTTTAT ACCAAAACCT 1380 GGACTCTGCA GAAAGAGCTC ATTTAAACAG ACCATAGAAC ATCGACACAC CATCGATGGC 1440 ACATGGTGGG CACTCCACAC ATGGTAAGCT CACAGGGGCC CGCCCAACCC AGAAGGTAGA 1500 CTGAATACTC 1510
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