Tag | Content |
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EnhancerAtlas ID | HS116-35274 | Organism | Homo sapiens | Tissue/cell | Left_ventricle | Coordinate | chr9:124424590-124426280 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr9:124425281-124425302 | AAAAGGAAAAAGAAACTCAGG | - | 6.31 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGACAGTGT GGTCTACTGG CCAAACCCAG CCCCTCATCT GTTTCTGTAT GACTTGTGAG 60 CCAAGAATAG TTTTTACATT TTTAAAGGGT TGGAACAAAA AGTCAGAAGA AGGAGAACAT 120 AGGGAGTTAT ATGAAATTCA AATTTCAATG CCCATAAATA AAGTTTTATT GGAACACAGC 180 CATGTTCATT CATTTGTGTA TTGTCTATAG CTGCTTTCAC GCTACAATGG CAGAGTTGAA 240 TAGCTGAGAC AGAGACCATA TGGACTTGTA AGCCTGAAAT ATTTGCTATC TGGCCTTTTA 300 TGGAAAGTTT GCTGACGCCC AAGATACAGC TAAAGCCACC TACTCTCTCT CCAGGCATAA 360 CTGGCCACCT AAAGGTGGTG GGTATCCTGC CTACATGTGC TTTCTGCTTT TACATAGAAG 420 CCTATGCTTC CAAGTGTGTC GAATTGCATT GTGTGTTTAA AAATGGATAT GGTGAAATTG 480 CACATGGCAG AGAGGAGCAA ACACATATGG ACACCCTGAG ACCTCCTTAG TTTCCTGAAC 540 TCCAGCAGCA CAGAGTAAAT GCCAGCTCTC TGCCAGCCCT GGAATGGGCC CTGCAGATGC 600 AGAGAAAAGA ATCGTGGGAA GAAAACTCCA GAAGAAAAAA TGGGGAAAGT GACACTGCCG 660 ACTCAAATTA CTAGAAATCC TCAGAAAGTA AAAAAGGAAA AAGAAACTCA GGGTTGAGAG 720 AAGACTTTGG GCCGGTGAAT TCATCCTTGG AGTGTTCAGG AAATCCAGAG ATTTTTGGAA 780 GGCTGGGAAT TCTTTGGAAG TGAGGCGTGT CTGGAGATAA GGAATAGGAA GCATGGGCTG 840 TCAAAAGCAA TTGTTAGGGA GCTCAAGTAG AGAAGCAAAA GGAAAACCTG GGGACAAGGT 900 CGACAGATGC TGAAAACCTT GTAGGATTTA TACTAGGCTA CACCAGACTA TTAACGCGGC 960 CAACCAGAGA CCAACAAGGG AGCAAACCCT TGCACTGTCC TTGCGGAAGG GCCCTACCCA 1020 GCATCCTGGG ATGTAACTGG GAAGGATGTG TCTCATTAGC ACCTCTGCCC CACCTCTGGA 1080 ATACCAGCTC CAAGCCAAAC ACGTCCCCTC TGAGCAGCTG CTGTGCCCTG CCCCCGAGTG 1140 CTCTATGTTG AGGATCCTCC GGGCAGGAAT GGTGGGCTGG ATGCTGAGCC CTCTACAGTT 1200 GTCCCCATGT CCCTCTCCCA CCAGACTCCA CTCCCCAGCA GCAGTGGGCA ACCTCCTCTG 1260 ATTCTGAACC ACCTCCTGAG CTTACAGACC ATTGGAACTC GATCCCAGTT CCCTTTAGGA 1320 GACAGCAGGC TATCATAGTT CCATGGCCTC AGGACACTGT ACCTGTACCA CCTCCAAACT 1380 CAACATCATA AAACCAAAAC GTGAAATCAA CATCCCTCAT CTCTTTCTGC CAGGTAGCTG 1440 GGACTGAGCT GGGCCCTGGG GACATAGAGA GAGGCCAAGG GCCAGGCGCG AACTCAGCTT 1500 CCTGAGTCAC TTGGGAGCAC TGTCTTCTCA CTCATCTCTG CACAGTGCCA TTCCTTTCCC 1560 ACATTGGGGC AACCCTTAGA TTCAGAGATA TCCGGGCTTG AATCCTGTTT TCAACGTTTC 1620 CTAGCTGTGT GGTCATGGTT TGAACTTCAG TTTCCTCCGA TTAAAGGTGG AGCTGATGTT 1680 TCTTAATTCA 1690
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