Tag | Content |
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EnhancerAtlas ID | HS147-03518 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:167012760-167014100 |
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 | TAAGGGTTCT CTCAATCTCT TTCTGGGGAA AAAAAAAAAA TCTATAAGAC AGCCCAGAAC 60 TAACATAGTT AGACCTGAGT TTGGGCTCTA TCTTTGTCAC TAACCAGCTG CATGTTCCTT 120 AACAAGTCAC TTTAATATCC CGAGCGTTGG TTTCCTCATC TGTAAACTAA GATGAATAAT 180 GCCTGGCTGA TAATGTGGCT GTGAAGATTA AAATGGGTCA TGCCTTTGAA TATGCTTTAT 240 AAAATTCAGT TCTTCTTTCA TTTCCTCAGC CGATTGCTCA TGTTCCTCTA ATACACTGTC 300 CCCACCCTGG ACAACCTCTA GCAGGTATAT GCACACCTGA AGATACTGAG ACAGGGAGAC 360 TGACTAGTTG AGATTCACTG AGGCTGATGT GTCTAGAAAG TTGCTCACTA AGTATTCCCG 420 CAGGGTGTTT GAAGCCTCTT CCTGGATGCC TGGTGAGACG AGACACTTTG AATCCACCTT 480 GCAAAGCTCC TGCTCCAAGA CAGCTGCAGC TTGTGCTCTG TAGAGCGATA TGAAATAATT 540 GCCCGTTGGC ACAATAAGCC CATCTCCTCT CCGGGCAGCA CAAAAGAAAG CTCAAAAGCA 600 TCTCCGGTTT TGATTGCCAA GTGGGGGAGG CAGTGAAAGT ACACTAAATT ATGAGTCCAG 660 GTGCCTCTCT ACAGAAATCC ACTTCCGCCT CGCTGCCGCT CTGAAGGCGC GCAGTGGGTG 720 TTGACGTCAC CTTCGGCCAC AGGAGCTTGG AGAGGCTGGG GCCCTGACTC CCCGCGGGAT 780 CCGCTGGTAG ACCAGGGCGT GCTCTCAGAC TGGAAGTGCA GGAAGGCTCG CTTACTCTCG 840 CCATAGACCA GACTGACAGG GGTCTGCCAA GGCTGCTGGG AATGTGGGAA GTGAACTTTA 900 GGTGGAAACA GAAAAGCTTC TCTCTCCGTG GGTAGCCTTT TTTTTTTTTT TTTAGTTCAG 960 GAGAGAAAAA AAAAATCATA GAAGCCTGCC AAGCCAAATA AACTATGCTC AATTAAGTCT 1020 TTCAACTGTG CAATTCCTCT TGTTGATTTT ATGAGGAAAA GGGCAGAATA GAAACATGAT 1080 GGGCTTGTTT AAAATACTTC AAAAGGGAAG AACCTATATT CTCCTGCTTC CCAGACCGAC 1140 CTCTTTCGGG CTTTCCTTTC CTCCAGCCAT GCTGCAGGCC TTTCACTGTC ATCTCCTCCA 1200 TCTGTGATAA AGCTGTCCAC AGAACCCGTC CTCAGCTGCT TTCTCACCAC ACACCCTCAC 1260 TCAGGGCATG TCCTCCATGT CATGCCCCTC ATCCAGGCCT GTGACTCCCA AGGAGCTGAA 1320 TCAGCCAAAA CTCTCCCTCC 1340
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