Tag | Content |
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EnhancerAtlas ID | HS139-03907 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr1:178498990-178500130 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata1 | MA0035.3 | chr1:178499984-178499995 | TCCTTATCTCT | + | 6.02 | SOX10 | MA0442.2 | chr1:178499811-178499822 | TTCTTTGTTTT | - | 6.62 |
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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 |
GH01I178530 | chr1 | 178498781 | 178499981 |
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Enhancer Sequence | CTGACACATT GACTAACACT TATCATGTCG AGGCCTGCAA TGAAATGAAT TTTGATCTAC 60 CTTAAAAAAT AAACAAATGA CTTACAGTTA TTTTGAGAGG AGGTAGGAAA TAAAATAATA 120 GGAAAACGTG AGTGGGTGGG GATCAGGACT GGCTATTCTA GAGGACAGGG GTGGGTCCCT 180 TGTAACACAG CATCTCACTC CTGTCAACCT GGTGGCCAAT GACAACAGAG TGAGGGGCAG 240 TTGGCTCACC CCAGCCCTCC CATAGGTAAC AGGTGCGGCA GCCCCAGGCC TTGACGCATG 300 TGGTCATCAG AGAAACATGA GGGTGAGTCA TCTGGGAGCA ATTAAGAGGG GAGGCCCAGG 360 AGGAGGCCAG ACTGTGTCAT CCATCCCATC ACTGCCACAG CACTGGCCCA GTGCCCACTC 420 ACAACATTCC TTCTCCTGGG TCACAGGCCA CAGGCCAGCC CAGAAGGTGG CTGAGGATGG 480 GCTCAGGCAT CCAACACTTC TGACTGGGGC CCAGATCCAT CTCTCTTAAA CTCAGCAGCT 540 CTGAGGATCC CCCAATTCCA TGGCAACGGG CTGCCTACCC ACCTTCCCAA GGGGTGCTAC 600 TCTGACTTGC CACAGTCTAG TCTCAGCAAA CTGAAGCTGT CCTTTAAAAA CATAAATTAG 660 AACATGTCAC TCTTCAGCTC AGAACTTTCC AGTGTTTTCC CACTTCTCTC AGAGCAAAAT 720 GCAAAGTCAA TGGTTCACAA AGCCCTACAG GATCCGCCCT GCTGCCTTCC CCATCCCTAA 780 CCCTGTACAG TATTTCACTT GCACTTTCTA GCCATGCTGG TTTCTTTGTT TTTCTTCAAA 840 CACAACACAT ACCCTCTTGC CTCAGGGCCT CTGCACTTGC AAACCCTACC CCCTCTCACC 900 ACCCTGCCAC CACCATCACT AGAATTCTCA GCCTTCCAGT CGGCCAGCTC CCTCGCCTCA 960 AAGTTACCTT CTCAGTGGCC CCCAGTCCCA GCATTCCTTA TCTCTCTTAC TGTCTGCTTT 1020 ATTTTTCTCT CCAGCACTCT TGTCACCAAC TCACATACCA TACAGTTTAC TTATTTGTTT 1080 ATTGTCTGTC TTTTTCTACG AGAATCTAAG CTTTTTGAGT GTGGAGATTT TGTTTCTGTC 1140
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