Tag | Content |
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EnhancerAtlas ID | HS024-01144 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr1:167012990-167014100 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr1:167013258-167013269 | GACAGCTGCAG | + | 6.62 | Tcf12 | MA0521.1 | chr1:167013258-167013269 | GACAGCTGCAG | + | 6.14 |
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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 |
GH01I167043 | chr1 | 167012838 | 167014050 |
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Enhancer Sequence | TATGCTTTAT AAAATTCAGT TCTTCTTTCA TTTCCTCAGC CGATTGCTCA TGTTCCTCTA 60 ATACACTGTC CCCACCCTGG ACAACCTCTA GCAGGTATAT GCACACCTGA AGATACTGAG 120 ACAGGGAGAC TGACTAGTTG AGATTCACTG AGGCTGATGT GTCTAGAAAG TTGCTCACTA 180 AGTATTCCCG CAGGGTGTTT GAAGCCTCTT CCTGGATGCC TGGTGAGACG AGACACTTTG 240 AATCCACCTT GCAAAGCTCC TGCTCCAAGA CAGCTGCAGC TTGTGCTCTG TAGAGCGATA 300 TGAAATAATT GCCCGTTGGC ACAATAAGCC CATCTCCTCT CCGGGCAGCA CAAAAGAAAG 360 CTCAAAAGCA TCTCCGGTTT TGATTGCCAA GTGGGGGAGG CAGTGAAAGT ACACTAAATT 420 ATGAGTCCAG GTGCCTCTCT ACAGAAATCC ACTTCCGCCT CGCTGCCGCT CTGAAGGCGC 480 GCAGTGGGTG TTGACGTCAC CTTCGGCCAC AGGAGCTTGG AGAGGCTGGG GCCCTGACTC 540 CCCGCGGGAT CCGCTGGTAG ACCAGGGCGT GCTCTCAGAC TGGAAGTGCA GGAAGGCTCG 600 CTTACTCTCG CCATAGACCA GACTGACAGG GGTCTGCCAA GGCTGCTGGG AATGTGGGAA 660 GTGAACTTTA GGTGGAAACA GAAAAGCTTC TCTCTCCGTG GGTAGCCTTT TTTTTTTTTT 720 TTTAGTTCAG GAGAGAAAAA AAAAATCATA GAAGCCTGCC AAGCCAAATA AACTATGCTC 780 AATTAAGTCT TTCAACTGTG CAATTCCTCT TGTTGATTTT ATGAGGAAAA GGGCAGAATA 840 GAAACATGAT GGGCTTGTTT AAAATACTTC AAAAGGGAAG AACCTATATT CTCCTGCTTC 900 CCAGACCGAC CTCTTTCGGG CTTTCCTTTC CTCCAGCCAT GCTGCAGGCC TTTCACTGTC 960 ATCTCCTCCA TCTGTGATAA AGCTGTCCAC AGAACCCGTC CTCAGCTGCT TTCTCACCAC 1020 ACACCCTCAC TCAGGGCATG TCCTCCATGT CATGCCCCTC ATCCAGGCCT GTGACTCCCA 1080 AGGAGCTGAA TCAGCCAAAA CTCTCCCTCC 1110
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