Tag | Content |
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EnhancerAtlas ID | HS139-14434 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr13:26759880-26761070 |
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) |
IRF1 | MA0050.2 | chr13:26760361-26760382 | AAAAGAGAAGTGAAAGCAAGC | - | 6.18 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 26760200 | 26760326 | chr13 | 26760531 | 26760858 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I026185 | chr13 | 26759591 | 26762164 |
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Enhancer Sequence | CTCAAAAAAA AGTTGTTACT TAAAGTAATG CATTGTCAAC AGAAGTGTAG AGGCCATGAT 60 TCTAAACTTG TGTTCTCTAC GCCTAACTAC GAACCTTGTG CCTTTCCAAA ACCAAAGGTC 120 ACACTTCTGG AAAGTTCCTT CCTCCCTCAC ATTCAATATC TATTTAGAGA ACACACACTA 180 TGTCCTAGCT TCTGCTAGGT TCTGAAAATA CAGTAAGAGG CAAAAGAGCC ATAGCCCCTC 240 CCACCCCGTG CCCTTATGAA ACTTGCAGTC TACATAAACA TAGATATGAA ACAAACACAA 300 AATGTATGTT TTAACCCTAA AATGCGATAG GGAAGCCAGT CAGACGATTT ACTCGGGAGT 360 AAGAATTCAG GTCATTCACC AAGGCGCCCA TGTCAAAGCT TCATCACCCG CCTCGCGGCC 420 CTAAAACGTG TCAGAGTCAT GATACACACA ACGCAGAGGA AAAGTTCAAA AACAGATCTT 480 AAAAAGAGAA GTGAAAGCAA GCGATCAAAA CATTTCTGGA AATCTGACAC ATCTGGAGTG 540 CCGTGTGGAG ACGCCAGGGC GCGTGGAGCT TTGAGCAGTT AAAAACCCAG ACCGGGAGGC 600 CAGTGCGTGT GTAAGACCGC GTTTCTCTGC AAGGCTGTCC CGCGGCAGGA ACGCGCTCGT 660 TGGGCCGCAG AGCAAGAGCG GGACGCGCCG GGGGGCGTCT GCGTGGCACG TGGGCCCCGC 720 AGCCAGTCGC GCTACCGACT GGCAGTCAGC GGAGACGCTT CGGAGCAGGT CTGTTAGGGC 780 GCGCGCACAC ACATGCACGT GCACGAGCGC ACGTACACGC GCACACCGCC AGCGCGGACC 840 CTGACGGGGC CGAGCCTCGG AATTGGGCCT CCTCGGCCGC CGTCGTCTTC TCAGCTCTCA 900 CAGGGCCCGC AGCGGCGCTA TACCTTCGGC CACAGGTAGC GCGTTCCTTC GCTGTGCTGA 960 CCGTCGATCC CGGGGGCGCT AGAGCGCCGG CTCCGGGGAG GGCAGGGAAG CGTCAGGGAC 1020 CTTTCTTCTT CTTTTTTTTT TTTTCTTTTT TTGAGACGGA GTCTCGTTCT GTCGCCCAGG 1080 CTGGAGTGTA GTGGCGCGAT CTCGGCTCAC TGCAATTTCC GCCTCCCAGG TTCACGCCAT 1140 TCTCCTGCCT CAGCCTCCCG AGTAGCTGGG ACTACAGGCG CCCGCCACCA 1190
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