Tag | Content |
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EnhancerAtlas ID | HS118-03646 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr11:71211360-71212340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr11:71212111-71212124 | AGAGACAGCTGCA | - | 6.36 | Myog | MA0500.1 | chr11:71212114-71212125 | GACAGCTGCAG | + | 6.62 | NR2C2 | MA0504.1 | chr11:71211746-71211761 | GGAGGGCAGGGGTCA | + | 6.26 | Tcf12 | MA0521.1 | chr11:71212114-71212125 | GACAGCTGCAG | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr11 | 71211627 | 71211690 | chr11 | 71211465 | 71211936 | chr11 | 71211998 | 71212187 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I071500 | chr11 | 71211761 | 71211910 |
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Enhancer Sequence | TCTCTGAGCA GGTGGCCTGT AAAACGAGGG TGGATCAGTG GCAGGGGTTC TACATCTGGG 60 ACCGTTGACC CCCCGAGGAG ACATTAGGCG ATGACTGGAG ATGATTTTGG TTATCATGAC 120 TGGGCTGGGG TCTGTGCTCC CAGCATCCCG TGGGTGGAGC CCAGGGATGC TGCTGAATGT 180 CCTACTGTGT GCAGGATGGG CCCCTCCCAA CCCCACACCC AGCAGAGAAT TCTTTGTTCC 240 ACGTGTTGGT GGTGCCAAGG TTGAGGAATG CTGAACATTT GGGACTAGAA GACGTTTGGG 300 GCTGCATGGT TGTAAGGAAG AGATACTGTA TCTGGCTGAT TTCCGTGGAA AGGAACTTGC 360 TCAAAGAGTG ACTTAGAGGG TGGAAGGGAG GGCAGGGGTC ACAGGGTCTG GAAAGCTGGG 420 ACTCAGGCCA GGTGGCTGCT GCCCTATATC CCCTGCTGTG GCTGGACGGA GCCCACACGC 480 CACACCCAGC CTGGGCTGGA TGCCAATCTG CTCTGCCATC CCTGAGTCCC AGTGTCCCTG 540 GGTCACCAGG CAGTGGAGTG GCCAAGCCTC GGGTGATGGG CCCTGTCATC TGGCCACCCA 600 GGGCAGGAGA GGGAGCTGCC CCAGCTCTGG CCTCTGTAGT GGGAGGTGGG GGCTTGGCTC 660 CCACCAAGAT GTACTCAGGG GCGGGCTCCC CCAGATCAGG AAGGGGGTTC AGACACTATG 720 CAGCCAAAAG AGTGACGCAT GTGGGAGCAT CAGAGACAGC TGCAGGTAAA GGTGGAGACG 780 CTGCTGTCAT CTGCAGTGAC AGCTATGCGT GATCTGGACC CGCCCCTCCA GGCTTTTCCA 840 GCACACACGC CCAGCATCTG GTGGGGACTC TGGTAATTTA CTTTTTCACC TCTGGGACTT 900 GTGACCCGCT TTTGGTGCGT GCCAGTGTTT CAACAGCCCC ACAGTCCGTC TTTGCGGGGC 960 TGTGGTGTCA CAGGCCTCTC 980
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