Tag | Content |
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EnhancerAtlas ID | HS073-12219 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr6:29932060-29932890 |
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) |
DUX4 | MA0468.1 | chr6:29932191-29932202 | TAATTCAATCA | + | 6.14 | FOXP1 | MA0481.2 | chr6:29932208-29932220 | TTCTGTTTACTG | - | 6.02 | NFE2L1 | MA0089.2 | chr6:29932792-29932807 | ACTGCTGAGTCATTT | - | 7.29 | Nfe2l2 | MA0150.2 | chr6:29932794-29932809 | TGCTGAGTCATTTCC | - | 6.41 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_57150 | chr6:29932125-29934802 | VACO_400 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH06I029963 | chr6 | 29931647 | 29936405 |
|
Enhancer Sequence | AAGTGTGCCT TTAACAAGTA CTGAGGTTAG GAATTTTAAA AAGGAAATGA GGCCACTCTC 60 GGAAGATCCC CTCAGTTTAG CAGAACAGCT AGATCAATTT TTAGAACCAA ATTTTTATAC 120 TTGGGCTGAG ATAATTCAAT CATGAATATT CTGTTTACTG GGAAAAAGAC GGGAATAATT 180 AGAAGGGCAG CCATAATCAT TTGGGAGAGA CAGCAGCATC CTCCTGGGTA AGGAGTCCTG 240 CCAGCTAAGC AGAAATTCCC AAATGCAGAT CCTGGATGGG ATAATAATGA CCCCAGGGAT 300 CGGGTCCAAA TGCAAGACCA TAGGGAGCTA ATAATTAGAG GGATTATGCA GTCCACTCAT 360 AGGACACAAA ACGTCCCCAA AGCATTCAAG ATCCAACAAC AAGAAGAGGA GACTCCCTCT 420 GCATTTCTGC AGAGGCTCAG GGATCAAGTG AAAAAATATT CAGGATTAAA TCCAGAGGAC 480 CCAGTAGGGC AAGGCCTTTT AAAGGTTAAT TTTGTAACTA AAAGCTGATG TAATATTACT 540 AAGAAACTGC AAAAGATTAA CGGATGGAAT AAAAAACCAA TTAAGGAAAT ACTGAGGGAA 600 GCTCAGAAAG TTTGTGTGTG TGTGTGAGAG AAAGAGAGAG AGAGAGAGTT AAGCTGCTAT 660 ACCTGAAGGA AGAGAGAGCC AGCGGCACAG CTGTGTGTGG CAGCTGGCTT CTAAAAGCTG 720 TTGATAAAGG TTACTGCTGA GTCATTTCCG CAGAGCTGCC TGTTTTTGCA GACAGACAAG 780 GGGAGCCAGG GCACAGCACG GCTCGGCTCA TGCCCAGAGA AAGAGGAAGA 830
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