Tag | Content |
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EnhancerAtlas ID | HS043-27500 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr22:41448410-41449480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Hnf4a | MA0114.3 | chr22:41448708-41448724 | TGGGACAAAGTCCAGA | + | 6.15 | Nr2f6(var.2) | MA0728.1 | chr22:41448470-41448485 | TGAACTCCTGACCTC | - | 6.22 |
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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 |
GH22I041052 | chr22 | 41448391 | 41449582 |
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Enhancer Sequence | CTAGCTAATT TTTGTATTTT TAGTAGAGAC AAGGTTTCAC CATGTTGGCC AGGCTGGTCT 60 TGAACTCCTG ACCTCAAGTG ATCTGCCCAC CTCCACCTCC CAAAGTTCTG CAATTACAAG 120 CATGAGCCAC CATGCCCGGC CTAATGATTT TAAATATGTG TCAGTGGTCC CCAAGACTGC 180 TCTCAGGATG GATGATTTAT AAGGAGGACT CAGAGGACTT AGCATGTAGT CATTTTCACA 240 GCTAAGATTT ATTATAGTGA AAAGATACAA AGCAAAATCA GCAAAGGGAA ACAGCTCATG 300 GGACAAAGTC CAGAGAAAAC CAGACACAAG CTTCCAGAGT GCTCTTCTAG TGGAGTCAAC 360 ATATTACATA TCTAATTCCT CCAGCCGCAA GTTGTGATAA CATGCGTGAA ATGTTGTCTA 420 CCGGAGAAGC TCACTTGAGA TTCAGTGCCC AAGTTGTTAA ATTGGGGCTG GTCACGTATG 480 CACTCTCTGC CTAGCACATA CCAAAGTTGC AGACTCACAG AAGGAAAGCA AGTATTTAGC 540 ATAAACCACA TTGTTTGTAT AGTTTAGGCA CAGTGAGCCA CTCTTAGGAG TCCTGAAATC 600 CATTTCTCCA GACATTAACC AAGGGTCAAC CTTGAAAGCA TGAATTTCTA AGGATAGCAG 660 TCTCACGCCC ACCACGTTAA GTCTTTTCTA CACAAGATGT TAAACCAGTT TTGCATCATA 720 GGGATAAATT CCTTTGATCA TGGTGTGTAA CTGGTTTTGT TTTGTTTTGT TTTGTTTTTA 780 CAGACAGGGT TTCATTCTAT CAACCAGACT AGAGTGCAGT GGCAAGATCA TAGCTCACTG 840 CAGCCTTGAC CTCCTGGGCT CATATGATTC TCCCACCTCA GGCTCCTGAG TAGCTGGGAT 900 TACAGTCACA CACCACCATA TCTAGCTCAT TTTTTTGGTA TTTTCTGTAG AGACAAGGTC 960 TCTCTATGTT GCCCAGGCTG GTCTCAAATT CCTGGGCTAA AGCAACCACC TGCCTGAGCC 1020 TCCCAAAGTG CTGAGATGAG CTACTGCGCC CGGCCTGTAA CCCTTTTTAT 1070
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