Tag | Content |
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EnhancerAtlas ID | HS064-00256 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr1:26002060-26003280 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr1:26002631-26002644 | AGAAACAGCTGCA | - | 6.29 | Myog | MA0500.1 | chr1:26002634-26002645 | AACAGCTGCAG | + | 6.02 | Tcf12 | MA0521.1 | chr1:26002634-26002645 | AACAGCTGCAG | + | 6.62 | Znf423 | MA0116.1 | chr1:26002536-26002551 | TGCCCCCTGGGTGGC | - | 6.13 |
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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 |
GH01I025675 | chr1 | 26002283 | 26003398 |
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Enhancer Sequence | AATGACTTAT TTTGCGGGGG GGGGGGGAGG TGGTTACCCA GTGTGGGATT GCTGGATCAA 60 ATGATAGTTC TACTTTTAGT TCTTTAAGGA ATCTCCATAC TGTTTTCCAT AGTGGTTGTA 120 CTAACTTATA TTCCCACCAG CAGTGTAAAA GTGTTCACTT TTCACCACAT CCATGCCATG 180 GCTGCTTTTT ATTGAGCACA TATTATATAC GAGCCATTGT GCTCAACACT TTACATCTGT 240 TATTTACTCT TAGGGTTATT CTAAGGATTA AGTATTTCTG TCCTTTTACA GATGAGGAAA 300 CTGAGACTTA CAGGGGTTAA GTCACTCACT CAAGGCCACA CAGCCAGTAA GGTGGCAGAG 360 CCCTAGAGCA GCCTCTCAAG CTTCAATGTG CGTTTGAATC ACCTGGGGCT CTTGTTAAAC 420 TGCTGCTACA GATTCAGCAG GTGGGAGAGT GGAACTGAGG TACTCTGTTT CTGACGTGCC 480 CCCTGGGTGG CCCTACTCCT GGTCCCTGGA GCACTTTGAG CAGCGAGAGT TTCTCTGCCT 540 GTATGGCCCA CACTCTCGAC CCTGATGCCT TAGAAACAGC TGCAGACAGG ATGCGATTCC 600 TGAGACTGCT CAAACCTGAA ACCCCATGGG CAGGATGTGG GTGAGCTGTC TGGACCTCAG 660 GTGGGTGGGA GTTGTATCAT ATGCTCATTT CCCACATTGG CCTTTCAATA GCTTGAGTAA 720 ACCCGAAACT GAGAGGGTTG GAGGCAGCAT CTCCCCTTCT ACTCCCCCGC TTCACCTCCC 780 CGGGCAACCA AACCCCACCC GTGCCCAGCT TCTGAGCGAT AGACCTGGGC TGTGTATTTG 840 CAGGAGCCTC ACTGGGGTCA CCAACCAGGT CATGTTGTGT TGCCCCAATA AATGGAACTG 900 GATCAGAAAA TCCAACGTGG ATAGTTTTTA GGTGCCAAGC TGTCAGCTCT TCCCTTGGAC 960 TGTGCTGAAA GTGGAAGAGG AGAAAAAAAT CAACCCAATG TTCTAAGCTC TCTGTCTACA 1020 TAGTCATTAG ATCCCAGGAT CGTTAGAGAC CAAATCCCTT CCCACTTGGC CCCTGCAAAT 1080 GGGGCCAGGT GTCACTGCTG GGAGACGCCA GTAAGGCTGC ACGTCATGGT GTGAGCACTT 1140 GTCTTTAATG ACTGGGAAAA TCCATTTCCT TCCTTGGCAG CTTTGAATGT AGCAACTGTG 1200 GTTCTGGGTC ACTGCCAGAG 1220
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