Tag | Content |
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EnhancerAtlas ID | HS099-08299 | Organism | Homo sapiens | Tissue/cell | HSMMtube | Coordinate | chr16:1110800-1112200 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr16:1111282-1111295 | AGCAGCTGCCCCT | + | 6.18 | SP2 | MA0516.2 | chr16:1111636-1111653 | GGGTGGGTGGGACTGAG | - | 6.12 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 1111339 | 1111413 | chr16 | 1111418 | 1111468 |
| Enhancer Sequence | GCCGGTTCTC CTTGCTGCCA TTACTGCATT TATCTGGCAA CCCCGCACCA CAACCCGAGA 60 CCTAGAAGAC CCTATGCCCC AGGCGGGGCT GAACAGGACA GACCTCGAAG AGCCGGTCCC 120 CAGATCGGAC CGCCAACAAC CAGGCCGGAT TCCGCGCCTC CAGCCGGTCA GTGCCTTGGC 180 AAGGCAGGAG CGGGTGAAAC TCCCAGCCCT CCCAGGGAGC AGTCAGATGA TGACACATCC 240 ACACCCGTCC ACAGGGAGGG AGTGCGACAA GGCCTGTGGC TTTCTGCGCG AGAATCGGCC 300 AGTGTCCTTT GGGGCCCGGG ATGGGGTTTC AGCACCCACT CTCACTACCG GGGCTCGGGA 360 GGGAGGGCTG GAGAGCCTCC ATCTGGTGCC GTCGGTGGCC ACTCCTCAGA CAGCGCGGGC 420 GGGTTCGCAG GCCCTGGGCA AATGTGGTGT TGCCACAGCC CCGCCCTACA GGGACAGCGG 480 TCAGCAGCTG CCCCTGGCCC CGCCGTCCCT AATGAAGTTA TAGATGGCAG CTCTTAAATG 540 TCTCCAGAAA TGGCAGAGAG GCTCCCAGAG CTGACGTGCA AATAAATTGC TTCTCAGGCT 600 CGGACCACAC AATTCTGCTG GGACCAAGCA CAGGCCTGGG CCCTCCGGCT GCCCCTCAGG 660 GCCTGGCTCT GCTGAGAGGA GGAAGCCTGG CTCTTGGGAG GGGGTCTCAG GTGCCCCCTC 720 CATGGAGCCC AGCAACCTGG CAGGTGGGGG TGGGCACCGC CCCTCCCCCG GGACTCCATC 780 TCCCCGGCAA TCAGCTGCCT CTCCCTTCTC TGGGGCCCCA GGTGGTCCTC ATGGAGGGGT 840 GGGTGGGACT GAGGCCTGAG CCCCGGGGAG GAGCTGGCTG GTGAGCCATG TATCCCAGTG 900 GTCACTGCGG CCAGCCGGGG AGGTTGAATC CCAGGCCCCA GCACTCAGAA GCTGGTGGAG 960 TGGGTTGAAT TGAGCCCCTC CAAAAACGTA TGTCGAAGCC CTGACCCCGG GTACCTGCGA 1020 GCACTGGAAA TGGGGTCTTT GTGAATGATC GAGTTAAGAT GAGGTCGGAC GGGGAGGGTC 1080 CCAAAAGCAA CGACCGGCAC CTTGTAAGGA GGCTGCTGAC AGCAGGGAGA AGTCGGGCGC 1140 GTGACGTCAG AGGCAGAGAC TGGAGAGAGG CAGCCCAGGA ACACCACGGG TGGCTGGCAG 1200 TGCGGAGCGG TAGGGCCCTC CCCTGGAGGC TTCGGAGGGA GTGTGGCCCT GCGGACACCT 1260 CGATCTCAGG CTTGCGGCCC CAGGGCTGGA GGGGTCGCGT TTCCGTGGCT TTAGCTCCCA 1320 GTTCGTGGCT CTTTGTTATG GCAGCCCCGG GAGACTCACA CAGGCGGTGA CTGTGGACAG 1380 GACCCCTGAC CTCCGGGCCA 1400
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