Tag | Content |
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EnhancerAtlas ID | HS116-09105 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr12:122205320-122206740 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr12:122206416-122206437 | GAAAAAAAAGAGAAAGCACGT | - | 6.18 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 122206350 | 122206670 | chr12 | 122205366 | 122206325 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I121765 | chr12 | 122203081 | 122206677 |
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Enhancer Sequence | CTCCCAAAGT GCTGGGATTA CAGGCGTGAG CCACCGCGCC CAGCTGCCCC TGCAAGCTTT 60 AACTTCTGTG GTGAAATGAG CCCAGAGAGT GACTGCAAAT GGGTGTAGGT TTCTTTCTGC 120 AATGATAAAA AGGTTTTAAA ACAGATTCTG GTGACAGTTG CACAACTCTG TGAATATACT 180 AAAAGCCACT CAGTTGTGCA CTTTCAGTGA GTGAATTGTA CGGTATCTGA ATCACATCAC 240 AGTAAAATGG CTACATAAAC ACATGTGCAC ACAACCAGCC CAGAGCCCCG GGGTGTGCAG 300 ATGGACGCCT GGGCTTGTGA ATGCCGGGCC AGGGAAGGAG CGATTTCTAG CCTCACCCGA 360 TGTCACTGAG CTGTGTTTAT TGGTGGCATC TGTCAGAGCT GGGCTCTGGG CACGGCGAGC 420 TGTGAAATGA AAAGCTGCTG CTCAGTCAGG CTTGTTGCCT GGAGTCTGTG TCTGCCTCAG 480 GCTGCTCCTA GACAGAGGGC ATTTCTCAGG GGAGCTTTGG GAGCAGGACA AAGGAGTGTG 540 GCGCCTGCCA AGTGCTGAGG GCTGACGTGG CTCTGCAGAG CTCTGGGAAG TTGCAGAGAG 600 ACCTCCTGGT TGCTCTTCAA GCTGGAAGTT GGGGGATCTG GCCAACTGCC TTTGCTGTCA 660 GAAATTTGGA GCCCAGGGGC TTCTTAGACT CTGACAGGCG AGACTAGGAT ACATGAGTGG 720 AGGTGGGAGT TTTCTGGGGA CAAAGAAGTA GATGGACATC TCACCCTGTC CCCATGACCG 780 CACGTGGCAC CTGCAACAAT CTCCTGTCAC CTCTGCGCTG GTGGCATCCA GATTAGCTGC 840 TGCTTTCACC AGCCACACCT CCCAGGCATC ATTCATGTCA ACATTTATTG AGTGCCTGTT 900 GTTTACCTGG TGCTGTTAGT GCTGTGAACA CAGAGCTGCA TAAAACCTTG CCCCTCAGCA 960 TAACTCCTGG GGAACACACA GGCTGTTGCT TGAAAAGCCA ATTTATGCCC AGAACTGTTG 1020 CATGGGCCGT CAAGGGAAGA GTGATGGTTT AGATCCAGTC TCGTTCTTAC GATGTGCGTA 1080 TGCGAGACCC TGCCTGGAAA AAAAAGAGAA AGCACGTGGG CGTGTGTGTG GACCCATTTC 1140 CCTGCCCAGT CCCAAGAGAG TTCTGGAGGG ATGAAGGTTA ATGACTGTTC CCACGAGCAT 1200 CCCCAGCCTC CACCTCCCAG TCCTGGGGAG GAGGGAGTTG GCTGCTCCTG GGTGCATTTG 1260 GCAAGTTGCT GCCATGTGTT TGGACTAGAG GAGCCTGGGG AGGCCAGCCA AGGCCTGAGA 1320 CACACTCTGG GATGTTGAAG GTTACAGGGT TGAGGGGTCC AACTCCTTTT TTCCTAGGCT 1380 GCCCCTGATG CTGGGGGTGG GGGGTGACAA CCAGGCTCTA 1420
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