Tag | Content |
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EnhancerAtlas ID | HS139-52762 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr8:22605130-22606570 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TEAD1 | MA0090.2 | chr8:22605839-22605849 | ATGGAATGTG | - | 6.02 | ZNF263 | MA0528.1 | chr8:22606178-22606199 | GAGGGAGGGTGGGGAGGTGGG | + | 6.82 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 22605286 | 22605400 | chr8 | 22606038 | 22606156 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I022741 | chr8 | 22599459 | 22607261 |
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Enhancer Sequence | TGAGGGGTGG CAGGGGGACC CTACGGGATG TTGCTTTTCA GCCTGGCGCT GCCTCGCTGA 60 GTAGCCTGAG ACTAGGAAAA GGCTTAAAGA ATTCACAGTG GGAAGGCTGC AGCCTGACTC 120 TGCTCCTGGC CGGCGTTTGC CCGCTGCCTG GCCCTGGCTG TTCCAACGAT GGACTTCCTT 180 CCTCTTTGGC CATAAAAGTC TCCCGGAAAG CCTTCCCACA GAGGCCCCGG GGGCTTTCTC 240 AGGGAATGTG TGAGTGTGTG CTCACACAAG CACTGTGGAG CAGGAGCCCA GGGCCGCGTG 300 CAGGCTCTCC CACAGAGCTG TGGGTCCTGG CGCTGGAGGA GAGGTTCGTC CCAGCCTGGG 360 TGGAGAGCGG AGGAAAGGCT GGCCCTTGCC TGGACTTGGG CCCTGGCTTA TGCAATGCTC 420 AGACTCTTAG TCAACTTCAG CAACTGGGGC ACATCCACAC GCATGTGCAC ACACGTGCAG 480 GCACACACCC GGGCAGGGAG GTGTGAGGAA GGGAGACCAA TGAGCCTGTG CCAAGCTCTG 540 CTTACAGATC TCCCCAGATC TGGAGAGAAA AGGGGAGCCC TTCTCCAAGA GGGGGCTGCG 600 CTCAGGCTGC TAGGGTATGA TGATGGCTCC AAGCCTGTGG CTGAGGTTGG ATGGACCATT 660 GAGAGGAGCC CTCCAGGGTG AGGGGACAGA AGCCCATCAG TCCGTATTGA TGGAATGTGG 720 CTACAGTGTG GAGAGAAGAA GATACTTTCT CTTCCTGCCC CAGAAGGTAC CCAAGCCTCC 780 GGGATGCTGG GTCACAGAAC CCGCCTGGCA GAGAGTTGCA TCAGAGCGAA ACTGCATGCT 840 AGATGCCTGA GGGGAGAGGG CACTGAGGAC TTGTGATCCT AATTTCCCAA CCTTCAGCTG 900 CTCAGGGTCA AGTCCTTAGG CTCCACTTGC TCTTCTCCCC TCCCCAGCAT TCTTCTGTAC 960 TAGGTTGCAC ATGATGAGGG TGGTCTGAGG GGAGAACAAG GAGGGGGTGT GACTCAGAGT 1020 TCACCCGGCT GTCAGCAGCC CTGAGTCAGA GGGAGGGTGG GGAGGTGGGT GGAACAGCTT 1080 TTGGTAGTCT TGGGGTTCCC TATAAGCAAG AGCATCCCAG AAAAATAGAA GAGAGCCCCC 1140 CAGAAGCTAC GAGGCTCCCA CATGCAGGGT AGGCCTTTTC TCGGCCACCA CTACACACCC 1200 CAGGAGAACA GGAGAGGCCT CCACGAGTCC TGGATGATTT AGGTGCGGAC TTGCCTGGGG 1260 GAAGGGTGTT GGCCCAGAGG ACCCCTTGGG TACCTCTGAA CTCTGGGATT CTGCAGAGAG 1320 GCCTCACCAC ATCAATGCTT TTTGCTCTGT GTACCCAGAT GGGTCTGTGG AGAATTTGGG 1380 GGGTTCCACT GCTGGGACTG GGGAGATGAC AATCTGGGGT CAGGGGACTG AGGTGGGTGT 1440
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