Tag | Content |
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EnhancerAtlas ID | HS116-08937 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr12:111176060-111177110 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-5 | MA0063.2 | chr12:111176901-111176911 | ACCACTTGAG | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr12:111176908-111176923 | GAGGTCACGAGTTCA | + | 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: 2 | ID | Chromosome | Start | End |
GH12I110738 | chr12 | 111175981 | 111176130 | GH12I110740 | chr12 | 111176406 | 111176810 |
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Enhancer Sequence | GGATACAGAG GTATGATCTT AAAATATCAA ACTCTATCCT GGAATTCCAT AAGCTCCATG 60 GAAATGAAAT CCTTCCTTCT TGGTCTTGAA TGACTTTCCA GTTCTTTATC TACAAAGCGA 120 CTGACACCCA GAATATTATC TCCTTCATAT TTTAATCTCT CAGGTCAACT AATGGCCTCA 180 ATTGTAAATT AAGTTAAATG GTGAAGTCCA CATAACATCA ATAATTTCCC TGCTTCACCA 240 TCAGGAATCC TCACCTAGTC AAGTGGGCTG ACTGGTACTG TGATTCTGCA CAACAGGTTA 300 CAGGTTGTAA TAGGACTGTG CTTTCAAAGA CATCAAATCA CCTCACTAAT TTCTACAGCT 360 GACCACTGCT GGGCTACAAC TGCATGTCCA TTTGCCCAGT TATGAGGAGG AACACCCTAG 420 GCTCAGAATG CAGAGCGCTC CTGTGTGTCA CATCCCCCGC AAGCACAACG TCACACACAA 480 TTCTGTCAGA TTTCACTGCT GCCTCCTGCT ACTGACAGGC AAGAGGGCAC TGCGGGCACA 540 AGGAGAGTAA TCCTTTTTCA ATGCTGTGGT TTAAAAAAGG ACTCCTGCAA GCTGCAGATC 600 ATCTGTCTCC AACAGAGCTT TCCCACCTTG CCTAGGAGGA GAGGAAGTGG GCATATGACC 660 AACATACTGA TGGGAAAGGA AGGGCAAGGG CTCACATCAG AGTTCTTATC AATGAGGGAA 720 TTAGAAACTG ACAACTTGGA TGTGAGTGTA AAAATTACCT GCTCTGTAAA CAAATAATTA 780 CAGGCTGGGC ACGGTGGCTC ATGCCTGTAA TCCCAGCACT TTGGGAGTCT GAGGCGGGCA 840 GACCACTTGA GGTCACGAGT TCAAAACCAG CCTGGCCTCA TCTCTACTAA AAATACAAAA 900 ACTTGGCCGA GCGTGGTGGT GCATGCCTGT TAATCCCAGC TACTCAGGGG GCTGAGACAC 960 CAAAATCGCT TGAACCCGGG AGGCAGAGGT TGCAGTGAGC CAGGATCCCA CCACTGCACT 1020 CCAGCCTGGG TGACAGAGTG AGACTCTGTC 1050
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