Tag | Content |
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EnhancerAtlas ID | HS139-00384 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr1:11399340-11400790 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LBX2 | MA0699.1 | chr1:11399704-11399714 | GCTAATTGGC | - | 6.02 |
| | 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 |
GH01I011339 | chr1 | 11399268 | 11400731 |
| Enhancer Sequence | CAATCGCCAA TGAACAATGA GACAGCGTGG GGGTGAGACG GGAGGACACA CCGGGAGGGG 60 CGCAAGAAAT GCCAGAGGCA GGAGACAGAT GGGTCCAAGG GCCAGAGAGC CTGCTCCAGT 120 GGCTCCTCGG AGTGAGATGG GTCAGAGAGG GAGGCAGGAG ACCAGAAAAT ACCAAGGAAG 180 AAAAATCTAA GGTAAGGGAG ACCAAGAAAG AAAGAAGAAG GAGTCAGACG TGCAGCTGCA 240 GGGACAAAGA CACATAAACC GGGGGTGAGA GAGACAGAGT GAGAGTTGCC TCCAGCTGGG 300 GCTGGGTGGG GAACTTAGTT CCCACCAGGG TTGTGGACTT GGGAGCTTGC TTGCGGGGAG 360 GAGGGCTAAT TGGCGATTTC ATCCAGGTCC TCCAGAACGT CTGCAGAAAA ACAAACCCGC 420 TAAACATCTC TCACCGTCTG TCATCTTCAT TTTGCTTTTG TCTTCAGAAT AAAGAGAATC 480 TGAAACTCCC TAGGAGAAGC GGCTCCAGCG GCTCTCAGGC TGTCTCCCGT TCTGCTCCTT 540 CTTCATGCTT TTCTGGTTGG AGTCTTTGTT CCGCAGCTTC TTGCCCTGGT TCAGGCTGGC 600 GGCTGCTCTG ACCCGGCGTG CTGGGGTCTC CATCCCCATC TCTGTCACAC TGTGGTCTGG 660 AGTGTCTGGG TCTCTTGCTC CCCTCCCCCT CCCCCCAGGC TCAGCCTGAG CCACCCCACC 720 CCCCTTGGCC CGCGTGGCCG CTGCTGATCC TTGCTACTCC CAGCTGTCTC CGTGGCTCAG 780 CCTGCAGATT GACAGGGCCC ATAAATCACC GTGGCAAGGC AGGGCCCTGG GAAAGGAACA 840 CGGGGCCAGG TGCTGACAGG GCTGGCCTTG GGAGCTGGGG CTTTCGGCTT TCTGGTGAAT 900 CGCTGGGGCG TGGAGCCTGT GGCTTCTCTC CCAGCTAAAT GGAGCATTTT GGTTGCAGTG 960 CCTGTGTCTC CTGCCGATTT TCTCCAGCTC CCTGGAAGGT GGGACAAGAA GAAATAGGTT 1020 GAATGTGAAG CAAGTGGGAT TCGGGTTAGA CTGAAAAGAA GAATTTGCAG TGATGAGGCT 1080 TAACTTTGGA AAGAGGAAAC ACTGGGATGG GAAATGGTGA AACCCCTTGG CAAGGAGTTG 1140 GTAAAATCTG GATGGATTCT GTCTGATGAT TTATAGTGCT GCCTGGAGAC AGGGGAATGA 1200 AACATATGAT CCACTCGACA CAGAAGCCTT TGCTTTGTTT GAGGGGAGCC CGGGGGCCAG 1260 GAGAGCAAAG AAGTTACCAG TGGGGGCTTG GGGAACATGC AGCTCCCCTC CTGACCTGCT 1320 GTGTGATCCT GAGCAAGTGA CTCAACCTGG CTGGTCTCTA TCTGTAAAAT GGGGATAGTC 1380 CCACTTCGTA GACTTACCAT GAAGCTTAAA GGGCAGTGTA TGCAAAGGGC TCTGCACAGT 1440 GCTTGGCACA 1450
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