Tag | Content |
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EnhancerAtlas ID | HS139-37155 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr3:49333930-49335300 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr3:49334417-49334428 | TGGGTGTGGCT | - | 6.14 | MSC | MA0665.1 | chr3:49334834-49334844 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr3:49334834-49334844 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr3:49334834-49334844 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr3:49334834-49334844 | AACAGCTGTT | - | 6.02 |
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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 |
GH03I049296 | chr3 | 49334281 | 49334430 |
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Enhancer Sequence | AATGAGCCAG GCGTGGTGGC GGGTGCCTGT AGTCCCAGCT ACTCGGGAGG CTGAGGCAGA 60 AAAATGGCAT GAACCCGGGA GGCAGAGCTT GCAGTGAGCC GAGATTGCGC CACTGCACTC 120 CTGCCTGGGA GACAGAGCGA GACTCCGTCT AAAAAAATAA AATAAAATAA AATAAAAATA 180 CCAGATGCTA CTATTGCTTT CATAAAACAA TTGTCAATTC AAATTCATCT ATAAAAGAAT 240 TTGTTTTTCC AATGGTTGGC CCATAGGCCC TCTGAAAATT CCTTTGTTGG TGGTCTGCTA 300 AGCTCCCCAC AGGGTAATCC TCCAGTTCCT TTCAGCTCAG GTGTGTGAAA ACACTACTTT 360 CTGGAATTTA CAGAGACCAT GTTAAGGGCT TGGGGTTATA TGTGAAAGTG GACTTTCCCA 420 TGTTCTAGCC CTTGGCACAG TGTCAGCTCT TGGCTGTGTC TGTGCAAGTG AGAACAGAAA 480 TAGATCTTGG GTGTGGCTAG GAACTATTCC TTTTAGAGAG ATCTAGAAGT CATAGGCCCA 540 AAAATGTAAA GGGAAGGAAC TATCTCCTTT ACATACTGAA TTCCTCAGCC AAAAACAAAA 600 ACCAAAACAA AATCCTAAAA CCCTTTCTCA GCAGAGGCAA GTTCCTGAGT GAGAGGTAAA 660 GAGGGAGGGA CAGTACGGCT GTGCTCCATA CTTCCTGGGC AAGTGGCTGC CTGGGAGCAG 720 CAGGCAAGTT CATGTATGGG AGCAGCCGGC AAGTTATTAC ACCACTGTGC CTGGAAGAGG 780 GACACACACA CAATTACACA GAGCAGCCAT GAAGCAGCAT GTGGGAAGGC AGAGGAGGCC 840 TTTGTATTGT CCTCACAGAG ATGAAGAAAC TCAGTCTCAG AGCTTACAGA ATGTTTGAGC 900 TGAAAACAGC TGTTTAAATC AGCCCTGTCA TTTCTGCATT GGGGATGGTA GTATCATGGT 960 ACTCGCTGAG AAGCTACAGC CTGTGGCAGA GAAAGGACAA GATCCTTCCG TACCACACCC 1020 CTACTACCAT CTTCCCATCA CACAGCTGGG ATTCCTCTTA AGAAAGGCAT CTCTGATGGT 1080 AGGACCATCT GTAGGAGCAG TGATTTGGCC TTCTTCATAG GCAAAACTGT TGAAAAAAGG 1140 CTGTGGCTGT GCTGAGGAGA GTTATCAGAA TGTTTAGCTC TGCAGGGCAG GAGGGGTTGA 1200 GCACTGATGG CTGCCCACGA TGCCCTCAAT ACCCATCTCT TGCACCCAGG GGTCAGGGCC 1260 AATCCACATG AGCAATGACT GCCCACATTT TTGTTCTGGA GATATGAATG CAGCAAAGTC 1320 TCTAGAATGT GTCCTCTGAC CTGACCTGCA GCAGAAACTG CTGAGTACTC 1370
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