Tag | Content |
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EnhancerAtlas ID | HS187-20627 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:7073470-7074780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr6:7074238-7074259 | AAACTCAAAGTGAAACCAATG | - | 6.62 | USF1 | MA0093.2 | chr6:7074157-7074168 | GGTCACGTGGC | - | 6.62 | USF2 | MA0526.2 | chr6:7074154-7074170 | CTCGGTCACGTGGCCC | + | 7.29 | ZNF263 | MA0528.1 | chr6:7074527-7074548 | GGAAGAGGAGGAGGTAGAGAG | + | 6.49 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr6 | 7073582 | 7073600 | chr6 | 7073600 | 7074227 | chr6 | 7074033 | 7074425 | chr6 | 7074275 | 7074702 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I007073 | chr6 | 7073441 | 7074728 |
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Enhancer Sequence | TGCCTGGGAC CAGAAATATG GACACTTTTA TCTGGCTGAT GGCCCATCAC GATTACTGCT 60 CTGTTCTCAC AGGGTTGAAC ATTTTACTCA CTTTACATGA TTTTAAACCA CTGTATCCCA 120 TTGACTTCTG TTGTTGAAAC AGAGGATTTT GGCAGCCTGG TTCATTTTCT CTTGTATATC 180 AGGTTCTTTG GGTTCACTAT TTTCTTTTTA ATAAGATCAT GATATTTCAG TGTTTACCTA 240 TAGCTCACCC ACCATTTAGG TTTTATTTCC AGTGCTCTCA TGCTTCCCTA AATCCTGTAC 300 GAAAGATGCT ATGTCAGGAG GCACGGTGAC TCAGGCCTGT TGTCCTGGCA CATAAGAAGG 360 CGAGGTCAGG TGTTTGAGAC TAGACTGAGC AACATAGGAA GCTCTCATCT ATTAAAAAAA 420 CAACAAAAAA ACCAAAAACA AAAAAACATG CTATGTCCTT GGCTATTCGA GCCACAGCTT 480 TGTGCATTGA CACACATCCA GCATCAGCAA GCTTTTTCTA AATGAGAACA AGCGTCATTC 540 CTTTGTCCAT TTGTCAGACT TGTCACATAT GTCTCTATGG GATTATAGTT TTTTTAAAAA 600 AAGAAAAGAA AGTAAAGGGG GAAATATCTG TAGGTTCCCC TTGCCTGTGT GTTCCTCTGC 660 TTTCAGCTCT TCAGCACAGG CAGTCTCGGT CACGTGGCCC TGCTCACGCA GGGCCCAGAC 720 CCACGCTGCG AAGCTCTGTA TGATTGTGTT TTGGGTTGCA GGAGGCAGAA ACTCAAAGTG 780 AAACCAATGA AAAAAACCAA TGTGTTCTTA ATGGTTTTTA CCTAAACCAT AAATCCCTCT 840 CTTCGAGGGA GAGGGGAATC ACCCAAGATT TGGCCCAGTT CCCTCATTAA GTTCCAGGGC 900 TATATTTGTC TGTATTTTTT CTTTTCTTTT CTTTTTTTTT TTTTTTTTTT GTTCATATGT 960 GTGTCAGTTT GGTGACGACC TGTGTCCAAC TCACTCAAGG AAGATATTTA AAATGCAGAT 1020 TCCAGGGCCT GATCTAGACT AAGGGAATAA GACAGTGGGA AGAGGAGGAG GTAGAGAGTT 1080 GAGTCTCCTG ACTCCCTGGT GGTGCTGACA GTCAAACAGG ACTTACTAAC AATGATGAAG 1140 GTATTATGGG CTCAGATTTT TATCCATCAC TACATTATCA CTAAATTTTT TTTTTTTTTT 1200 GAGACCAAGT CTCACTCTGT TGCCCAGGCT GGAGTGCAGT GGTGTGATCT TGGCTCACTG 1260 CAACATCCGC CTCCTGGGCT CAAGCGATTC TCCTGCTTCA GCCTCCCGAG 1310
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