Tag | Content |
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EnhancerAtlas ID | HS139-56929 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr9:119333600-119335090 |
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) |
CTCF | MA0139.1 | chr9:119334618-119334637 | GAGCGCCCTCTGTTGGCTG | - | 6.48 | EBF1 | MA0154.3 | chr9:119335009-119335023 | TTTCCCTTGGGAAT | + | 6.05 | EBF1 | MA0154.3 | chr9:119335009-119335023 | TTTCCCTTGGGAAT | - | 6.88 | SPIC | MA0687.1 | chr9:119334664-119334678 | GACTTCCTCTTTCC | - | 6.14 | Sox3 | MA0514.1 | chr9:119334209-119334219 | CCTTTGTTTT | + | 6.02 | ZNF263 | MA0528.1 | chr9:119334467-119334488 | TCTCTCCCTGCCTTCTCCTCC | - | 6.09 |
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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 |
GH09I116572 | chr9 | 119334280 | 119335170 |
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Enhancer Sequence | CACTCAATCT GGACTCCAGC CCTCCTTCCC TGGGTCTTCT CACTTTTCTT CTATTCTGTC 60 TCTTTTTCCA TCTTTCACAA CCCTTTCTCT TTCCCTATTT CTGGCCTCTC CCTCTTTTCT 120 CTTTTAGAAA CATTTACTGA ATTACAAGTG CTTTTGATCC ATGTGGAGTT ATGTCCATAC 180 GGTGAGTGTG AGTATTTGGT GTGTGCTGTG CTGTGGGTGC TACGTGAGTG GATGCCATCT 240 AATGTGTCTG TGTCTGTTTG TGCTGGGTGG ATCCATGTGG CACACGGTAT GTATATCTTT 300 ACAGTATGCC TGTGGGAAGG TGGCTATGTT TACGCATCTG TGTGCCTGTG CTGTTTATCT 360 ATGATACGCC TCTTGAGGCA TCTGTCATGT GTTGAGTACA AGCTGTGTGT TGTCTGTGCG 420 TGGCATGCTA TCCCCATGGT GTGTAACTTT GTATGTGTTG TGGATCTACT GTATGTGTCT 480 GTGTGCTTCC CGTGTGTGTG TGACCGTGTC TCTTTGTTAT CTGCCTTTCG TTGGCTGCAC 540 ATAGCTTGAA TGTCCCTGTT GGGTGATGTG CTCACATGCA TGTTTATATG TGTTGGTATC 600 TGTGTGTTGC CTTTGTTTTT GTTTAGCTGG CTGAGGTGAC TGCATTGTGT ATACCTGTAT 660 GGGATGGATT GCATTCATTT GTGAGTCTGC ACCCTATATG ATTTCTCTAA ATCCCCTGGC 720 TGCATGCTGT GTCTGTGTGG GGTATGTTGC ATTTGTTGTT TGTAGGTACA ACTGCATATT 780 CTGTGTGTTC CCCTGTGTCT CTGCCTCTGT GAAATGTGTC TGTGTGTTTT CCCTGCCAGC 840 TCCTCCTCCC CTTCGGGTGC CCCAGCCTCT CTCCCTGCCT TCTCCTCCCC AGGCTGTGAC 900 CACTCTCAGC TGACACCTCC GCTGCTCTGG CAACCCAAGA ACAGCCTGGA GAAAGGTCAG 960 CTGGCCGCCT TCCCCAGGGC CTGCCTGGAT CCTTGGACCC CAGTGTTGCG TGGTGTGGGA 1020 GCGCCCTCTG TTGGCTGTAT GGGCCATGAA CACCACTGGA AACAGACTTC CTCTTTCCCT 1080 TGCTGCTCAC CCCTGAGACT TCCAGCCTTC TTAATAAGGG ACTTTAGGAG AGGAATGGGT 1140 AGGGTCGCCT ATAATTTGCC GTTGAAAGCG AGATGTTTTG GAGAATGAAA GAGGGTGTGA 1200 ATAAGTGCAC TGAGATACTG AGTATTCGGC AGATGCGTCT TAAGCAGATG GTGAGGAAGG 1260 CTTCCCTGAC CGCCTACTTG GGTCTCAGCC CCATGGGCAT AAGCCAACAA AATGTGTGCT 1320 AGCCCTCACT GGTGAAAGGG TCAGCTATTC CCAATTTATG TTTGAGGAAG TCAGAATCTC 1380 AAATCTATGC TTACCCAATG ACTTCACGCT TTCCCTTGGG AATAATTTCC CAAGACCCCA 1440 ATTTCCCCTT TGCAGCAGGG ACCCAAGGTG GAGACCCAAG GGTTCCAGTT 1490
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