Tag | Content |
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EnhancerAtlas ID | HS139-51328 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr7:101245260-101247010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr7:101246679-101246692 | TTCCAGAAGGTTC | + | 6.15 | HSF1 | MA0486.2 | chr7:101246684-101246697 | GAAGGTTCTGGAA | - | 6.3 |
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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: 1 | ID | Chromosome | Start | End |
GH07I101602 | chr7 | 101245680 | 101246081 |
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Enhancer Sequence | TTGCTGGGGA CATGTGGACA GGCAGGGGCC ACCAACTCAG AGCGAAGACG TCACAGATGT 60 GTGAAAACAC TGAAGATGGG GACACAGAGG CACCGAGCGT TAGGTGGCTG GAGTCACTGG 120 ATCACAGCGT CTGGAGCCAA GGGTTTCCAC TGTTCCCAGG TGTAATTCCT CCCCGCAGCC 180 GTGCAAGGCG GGTGCCCCAG CTGTACTCAC TTGGCTGCTC TGTAGGTCGC ACAGTCAGTA 240 AGCGGCAGAG CTGGGACAGG CCAGGCAGGT AGGCGTCTTG ACTCGGTGCC TTACCCTCTC 300 TGGCCTCAGT CTTCTCATCT GTCAAATGGT ATAATAATAG GATGTACTCC TCAGGGTTGC 360 TGGGAGGGTT ACACACGTTA GTGCACACTG CCTGGGGCTC GGTGACTGTT CTCTAAGTGT 420 TTGCTGCTAT TTTTTTTTAC TTAAGGAAAC TTAACATCGA ATAGGTTAAG CAGCCGGGGC 480 TTGAATTTAG TCTTCTCTGC ACCAAAGTTG CGCTGTGGAC TCTTGTGCCG ACTGTGATCT 540 AGAGATTCCC AAGCCCCAGA GGCTTTGGGG AAGGCGGAGC CAGGAGAGGC TGCTCAGCTG 600 TCAGTAGATG GCGCTGTGGA GCCACAAGGG CCGCCCTCGC TGCAAAAGCC CGTTGACGCA 660 CCAGGCTGTG CACAGACTGG GGTCTCCCCG CCCTGGGCCA GGCCCTGCAC CAGATATGGC 720 CCCAGGAGAG GGGGTGCCGC TAACCCTGTT TCCCTGATGA GGGATATGAA GGCTCAGAGA 780 GGTTGAACCA CTAGCCTTGA GGTCACACAG CTATAAGGGG CAGGGCTGGG GCTCCCCACC 840 CCAGATGCCT CACTGAGCTC TCCAGCCCCA CCCCCATCCC ACCCCTCACC CTGGCCCTCA 900 AGAGGCCACA GTGACTCCCT GGCGCTTGAT GGGAGCCAGG CGCGTCCCTC CTTCCCCCAT 960 GGCTGGACAT TCCAATGAAG CTGAAGCCAC CAGCTTTGAA GTGAGAGCTA AACCCGGATT 1020 AGGGCGGCTC CAGGCTGGCC TCTCCTTCCC AGCCCCATTG CCAGGCCCAC GCTCACCAAC 1080 CACGTCAGGC CAGAGTCCTG GCGGCACAAA GGGGTCTGGG GCCTAGAGGA GGCAGGACCT 1140 GCCCCGCACA ACACAGTCCC TCTCATAGTC TGTTAAGAAG CCTCGGGGGC CCCCACGACC 1200 TGCTACTAGC CTGAAACCCC ACGTCACGCG GGTGCCAGCA CAGAAGCTCC CACGGGGCTG 1260 GGAGGCTGTG TGTCCGTCTG TCTGTGAGCA GCCACACTTC CCTGGCCTCA CCCTGCCTGT 1320 TTGGGTTCCA GGATCAAGCC TCTTTATTCA AGGAGATTTG GACTCAAGAC TGGAAGATGA 1380 CACTGGTATA GTGAAGCTAC ACCAGTTCTG GAACCCGTGT TCCAGAAGGT TCTGGAACAT 1440 CCACCTTCAA ATTAATCTCT CACAGCCTCT TCTTCAGAAT TCAGCTCTTC CCAGACTTCA 1500 CTTTTTTTTT TAATTTTATT TTATTTTACA GAGTCTCGCT CTGTCGCCTA GGCTGGAGTG 1560 CAGTGGTACA ATCTTGGCTC ACTGCAACCT CCACCACCAG GGTTCAAGTG ATTCTCCTGC 1620 CTCAGCCTCC CAGGTAGCTG TGATTACAGG CATGAGCCAC CATGCCCAGC CTTATTTTAT 1680 TATTATCTTT TTGAGACGGA GTCTCACTCT ACCGCCCAGG CTGGAGTACA CTGGTGCAAT 1740 CTCTGCTCAC 1750
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