Tag | Content |
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EnhancerAtlas ID | HS091-40790 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr6:31907100-31908720 |
Target genes | Number: 66 | Name | Ensembl ID |
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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) |
NR2F1 | MA0017.2 | chr6:31907137-31907150 | CAGAGGTCATGAG | + | 6.04 |
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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 |
GH06I031940 | chr6 | 31908021 | 31908270 |
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Enhancer Sequence | AGCCCCTGCC ACTGCCACCA CATTTGTTCT GCTCCTGCAG AGGTCATGAG ATCTTCAGCC 60 AGGGATCCCA GCATCTTAGC TATGGTCCAG AGCCACATGG TTTTATTTCT GCGTTGTTCT 120 GTACAAAGGC AACTCATGTT GAAGAGCCTG GGGTCAAACT ACTGCCCATG GTCTCAACCT 180 TACCTTCTTT TTTTTTTTTT TTTTTTTTAA GACAGTGTCT CACTGACACT CAGAGTATAT 240 TCCTGGAAAG ATGTCCACCC ATGCCGGCCC AGAAGCTGGT CCAGAAAGTA ACGATGTCCA 300 CCATGCCACC ATGAAGTGCA GTGGTGCAAT CATAGCTTAC TGCAGCCTCA AATTCCTGGT 360 TTCAAGTGAT CCCCTCAACT CAGCTTCCCA AAGTGGTAGG ATTACAGGTA TGAGCCACTA 420 TGCTCAGCCC GTCTTCACAA ATTTTTTAAA ATTAATTTTT AAATTTTTTT TGAGACAGAA 480 TCTTGCCGTG TTGCCCAGGC TGGAGTGCAG TGACTCGATC TCAACTCACT GCAACCTCCA 540 CGTCCTGGCT TCAAATGATT CTCCTGCCTC AGCCTCCAGA GTAGCTGGGA TTACAGGTGT 600 GTGCCACCAT GCCCGGCTCA TTTTTGCATT TTTAATAGAG ACAGAGTTTC ACCATGTTGG 660 CAGTCTGGTG TCAAACCCCT GGCCTCAAGT GATCCGCCTG CCTTGGTCTC CCAAGGTGCT 720 GGGATTACAG ATAGGCGTGA GCCACTGTGC CTGGCCAATT TTTAATTTTT TAATTATTAT 780 TTTTAATCAA CAGCTTTAGA CAGAGAACCT TGGTTTCATC TTCAGTGGGC TGTGGCCATG 840 GGCAGTTTCT TCATCTGCAA AAGGGGAGTA GTACTAGGAC CCAGCTCACA AGCTGACAGG 900 GGAAGATGCT CAGACAAACA CTGCCTGCCT GGCATAGAAA AATGCCCAGC ATATGTTAGC 960 CATGACCACG ACCGTCGTCG TTATCATCAT CATCATCATC ATAGCATCTC ATGTTTCAGG 1020 AAACTTTCCA GGAAGAAGGG ACCTCGATTC CCTCTGGGGA ATGTCCCTGG TGGTTGCTCT 1080 TTCAGCAGCA CAGCTGGCTA ACTAAGGCTT TGGCAGTTGC AGCCTCTAAA GGAAAAATTC 1140 CTCAGGTTCA GACTAAACAC AAATTGCACT GACCTTTGAT CAGAAAGTAA TTTCAGAGAG 1200 AGAGATGCTC AGACAGGGAG GGCAGCTGGT TTTGAGCCCC AACCTTTCAT CTTCCCCTTA 1260 GCTCCTCTCC TTTCCATTCA CACTGCCCCC TCCCCCATCA CCTGGCCCTC GGGGGTAAGC 1320 TGATTCCTCT TTAAAACTCT GGCCCAAGGA AGACAAAATT TAAAGCCCAC TCCCTTCCTC 1380 CTTAGCATCA CTGGACCAAG GTCAAATGCT ACAAAAACAT TTTATTGAAA ATAAGCAGGA 1440 AACCAAACGA AAATAGTCAA AGAAAACGCA CAAGGCACGA TCGTTGTCTA GCTCCAACTG 1500 TAACTGTTTC TATCTGGGCC ATTGCCAGAT TGCCTCCTGG CTGAAGATCT CTTGGTCCAC 1560 CTAAGCACCT TGCTTTTTAC ACACAACGCG GGGCTCTCTG AGAACAAAAA TGGGCCACAA 1620
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