Tag | Content |
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EnhancerAtlas ID | HS112-00616 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr1:90222880-90224080 |
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) |
HNF4G | MA0484.1 | chr1:90223491-90223506 | CAGGGACAAAGTTCA | + | 6.12 |
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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 |
GH01I089755 | chr1 | 90221267 | 90225158 |
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Enhancer Sequence | CAAATGCTGT CTTGAACTGC CAGATCGTAC CTTCGTATTT AAGAGACCAT TGCTCGGCAC 60 AACATGGCAG CTAATATTTA AAACAAATGG TAAAGAGGAA AGGCAATCAT TTCCTCACTA 120 AATGAAAAAG GAGATATGAA TCTGAGGAAC ACAATCCGGC ACTGATTGAA AGTAAATTAC 180 CAGTTGATTA GACGGCTGTA AATTCAGGGA GAGAAGCCTC AACCGGCAGC TGGATTTTGT 240 AAGGAAGAGG GCAATTAGAG AGGGCACAGG CGAGGCAGAG CACAGAGAGG GCTCTGCACA 300 GAGCAGACAG GGCAGCTTTG CAACACTAGG ATTACAAAGG CAGGAAGGGG TTTGTAGGAA 360 GTGTTCTGTG GATGGAGCCT GCAAGAAAGG GGAGCTCCCC ACTCCCACTC GCCCTGCCCC 420 ACCTCCCTAG TGAGCAGGAA GAGGTTAAAC TGCCAGTTCC CTGTCTAGCA GCAGTTAGGA 480 CGGGTGTTTG TTATTGCAAC ACAGGAAGTA TCACGATTTC TCTTCCTTTT TCAGGCTGTA 540 CTCAATCTAG AAGCTTTTTG CTTCCTATCA AAAGCCAGGG ACTTGAAAAC TACTCAGGTC 600 CCTGCAGCCC ACAGGGACAA AGTTCATGCA GATTTCAGTG GGAGATGCCA TCTCCGGATA 660 GCAACTGGGG CCAGTTTTTG CAGATGGCAA GCGCTTAAAG ATGCAAGCCT CCATGATTAC 720 CACGAACTGA GAAATCTCTG CAATTAGCAG GAGTGTAACT GGAAAACCAA GGGCTCCTCT 780 GTGCCTTACC AAAAGACATT CCCTCTTCCT CTGGCAAGTT GAAGAAGATA ATTTGGCCAG 840 CCTAGGAGGA AGTGATTGAT TGAGACAGAA ATGGTGGAGA GAAGGATGAC TGTGATTTTT 900 ACTTTGGTGA TGGGCATGAA CATAACAAAG AACAGATGGT GGATGCCTTA GTCCCACTGG 960 TGTTATCAAT TCCGTAGCCC TGAGCCCTGC CCTGCTACAG GCTTATGTAA TTCTCAAGCA 1020 TGTGCTCTCA TGGCCCAAGG GGAGACTATG CAGCACAGAC CCTCCAGCTG CGAGGTTAAC 1080 TCATCAATGC TCCACCCTTG TCATCTTTGG GTTCCAGCAC TCAGGCCCTG GATATGCCTC 1140 TCACCAGAAG TGAACACTTG GTGGGGGCTG CAATAGACCC AATGAACACA TCAGCTGCAG 1200
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