Tag | Content |
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EnhancerAtlas ID | HS007-14351 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr6:29931730-29932890 |
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 | CAGGAAACCA TCAGCTACGT GTTCTCTGGG TCTCTCAGAG AAAGACCCAC AAGAACAGAA 60 AACCAAACAC TGCATGTTCT CACTCAAATG GGAGTTGAAC AATGAGAACA CATGGACACA 120 GGGAGGGGAA CATCACACAC TGGGGCCTGT CTGAGGGTAG GGGGCTAGGG GAGGGATAGC 180 ATTAGGAGAA ATACCTAATG TAGATGATGA GTTGATGGGT GCAGCAAACC ACCATGGCAC 240 ATGTATACCT ATGTAACAAA CCTGCATGTT CTGCACGTGT ATCCCAGAGT TTAAAGTATA 300 ATAATGATAA TAATAATAAA TTGGATTTGT AAGTGTGCCT TTAACAAGTA CTGAGGTTAG 360 GAATTTTAAA AAGGAAATGA GGCCACTCTC GGAAGATCCC CTCAGTTTAG CAGAACAGCT 420 AGATCAATTT TTAGAACCAA ATTTTTATAC TTGGGCTGAG ATAATTCAAT CATGAATATT 480 CTGTTTACTG GGAAAAAGAC GGGAATAATT AGAAGGGCAG CCATAATCAT TTGGGAGAGA 540 CAGCAGCATC CTCCTGGGTA AGGAGTCCTG CCAGCTAAGC AGAAATTCCC AAATGCAGAT 600 CCTGGATGGG ATAATAATGA CCCCAGGGAT CGGGTCCAAA TGCAAGACCA TAGGGAGCTA 660 ATAATTAGAG GGATTATGCA GTCCACTCAT AGGACACAAA ACGTCCCCAA AGCATTCAAG 720 ATCCAACAAC AAGAAGAGGA GACTCCCTCT GCATTTCTGC AGAGGCTCAG GGATCAAGTG 780 AAAAAATATT CAGGATTAAA TCCAGAGGAC CCAGTAGGGC AAGGCCTTTT AAAGGTTAAT 840 TTTGTAACTA AAAGCTGATG TAATATTACT AAGAAACTGC AAAAGATTAA CGGATGGAAT 900 AAAAAACCAA TTAAGGAAAT ACTGAGGGAA GCTCAGAAAG TTTGTGTGTG TGTGTGAGAG 960 AAAGAGAGAG AGAGAGAGTT AAGCTGCTAT ACCTGAAGGA AGAGAGAGCC AGCGGCACAG 1020 CTGTGTGTGG CAGCTGGCTT CTAAAAGCTG TTGATAAAGG TTACTGCTGA GTCATTTCCG 1080 CAGAGCTGCC TGTTTTTGCA GACAGACAAG GGGAGCCAGG GCACAGCACG GCTCGGCTCA 1140 TGCCCAGAGA AAGAGGAAGA 1160
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