Tag | Content |
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EnhancerAtlas ID | HS114-00133 |
Organism | Homo sapiens |
Tissue/cell | Kidney |
Coordinate | chr12:122461520-122462440 |
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) |
Myod1 | MA0499.1 | chr12:122461644-122461657 | AGAAACAGCTGCA | - | 6.29 | Myog | MA0500.1 | chr12:122461647-122461658 | AACAGCTGCAG | + | 6.02 | Tcf12 | MA0521.1 | chr12:122461647-122461658 | AACAGCTGCAG | + | 6.62 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_39828 | chr12:122460562-122462503 | Jurkat | SE_47525 | chr12:122459729-122462496 | Pancreas | SE_58458 | chr12:122393066-122471220 | Ly1 | SE_58947 | chr12:122416318-122479345 | Ly3 | SE_60405 | chr12:122416330-122471265 | DHL6 | SE_61615 | chr12:122406328-122473788 | Toledo | SE_62898 | chr12:122406176-122468817 | Tonsil | SE_65468 | chr12:122460377-122463590 | Pancreatic_islets | SE_66606 | chr12:122460562-122462503 | Jurkat |
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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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Enhancer Sequence | AAAGAATTTT CAGAACCGTG AGAAGGGGAG GCTTTCCAAA GTTGAGATCC AAGTCGTCGG 60 TGTCTCGGGA GCTCCCCTGG TACACAGGGT GCCCGGTGCC CGACTGGAGC CATTTAAAAA 120 TGGCAGAAAC AGCTGCAGGC CAACACACAC ACGCTGGAAA ACAACCCGCA GCCCCCTCTA 180 CTGTGGGATT CCCCGCGGGA AGCCCGGAGT TGCTCCCCTC CTTGCCTCAG CCCCTGTGCA 240 AAGAAAGAAC TGGTGTCTGT GCCTGGGTCC CTTCTGTCGC CGGCCTGGAG GTTGGGAAAC 300 AGCCGGCAAG CCGCCTTTCT CTGCTCGAGG AGGCGTGGTG GGGCCTCCTA CTCCAGGTTC 360 CCGGCTGGAC AGAGGCTCCT GCACCCTGAC AGCTGCTCCC GCAGAGCGGC CAGCTGCTCT 420 GCAGGGAGGG CAGATGGAGA GATGGGGCTT CCCACCCCGC GGGCCCCGGG GCGGCCGGCC 480 TGGAGGCCTT CCAGCCCGCT GACCCCGCGG GGACCAGGCC TGTAGTTGGA GCTTGAGGGG 540 CTGTACCTCT GCGCCTCCCT GGGTTTGGGG AAACAACACA TCGTGTCCTC TGAAGACCTC 600 AGGCTTTGGG ATCTCATGGT CCAGCTTCCA GTTCACTTCG TTGCCGCGAC CTTGGGCATA 660 TCATTGTCAC TTCTCTAACC ATGGTGACCC GGGGTTTTGT GCTTGGCTTC CAGGTCCCCT 720 CGGGTTATTG AGGACGATTG AGGTCATGCC TCCGAGAGCA CCGCGCCCTG GGCGCAGGAG 780 GAGCTGTTGC TCAGTGTTGT CTGTGTTGTA AGGTGGACTT TGTAGAAACT TGGCTTTGAG 840 GTTTTTTGTT TTTTTTTTTT TTTGGCCCCT TCTAAGCGAA AGCCTTGGAC TTATTGCCCA 900 GGTTTCTCTG GCCCCTGAGA 920
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