Tag | Content |
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EnhancerAtlas ID | HS187-20981 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:30430980-30432350 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX3 | MA0684.1 | chr6:30431510-30431520 | AAACCGCAAA | + | 6.02 |
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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 |
GH06I030463 | chr6 | 30431461 | 30431630 |
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Enhancer Sequence | TTTGACCATG CTCCTCCTTC CTCACACTGT GGGGCCCCAG CTTTCCCTCC CAATTCCACA 60 CCCCCAGATG CTGGTACCAT GCTCAGGTTC ATCGTGGACA CCACTCCATC CGACATGGCA 120 ACACTTTTGA TCCAGCCGCT TTGACAACCT CGTTCAGTCT CCTCTGGAGA CAGCCACCCA 180 GACCTTTGCT GATGAGCTGG GACTGAGGGG AAAAGGCCTG CGATCTCTGA TGGGGTTGGC 240 AATGGACACC AAAGTCGTCT TCTAAAGACC AAGTACGCTC TAACCACGGA AATCGTCTCT 300 AACCACTGAC TCCTCCAGAA AAGGAAGAAA GAAGCCTCTC TACACTAAGC TGAAACACTA 360 AATACACTAA GTGTTGATTA AGTAGACTAG GTACACTAAG TGGTAAACTT GGTAAACTTA 420 GAGCACTAAG TACACTAAGT ACAATAAATG GTAAACTTGG TAAACTTAGA GCACTAAGTG 480 CACTAAGTTC ACTAAGTAAT AATATTAGTA CTAAGTGGTA CACTAAGCTG AAACCGCAAA 540 CCGCAGCCAT GGCAGAGGAA CCTCAGCTTA AATAGTGTGG AGCGGCCACT GGTTTCCGCG 600 GCTCGTAGTC GCGCCCGCGA GGAAACGCCA GGGAGGCTTC CTGCCCCGCC CAGCGGTGGC 660 CCAGGGCACA GGGAACCACG GCTGCTTCTC TCCGAGGTTT GTGGCCTGAG AAACTCTCCG 720 CTGCGAATCT GGGCTGGCCT CTCCGGGAAG CCTTGAAACT CAACTCCCGG GTGGGCCAGG 780 AAGGCTGCCC GACTTGGGCA GCGCCGGCCG GAGCCTTCTT CAAAGCCGAG CTGTTCGCCG 840 CCCTCGAGGC CCAGGCGAGC CTGGAGGAGG GACCGGGTGC GCTCAGATGG GGCCCTTGGT 900 GACTGGCGAC CCCATGAGCA CCCACCCTCC AGCCTGGGGC GGGATGGCCC AATCGGGCGC 960 TGTGGGGGTC CGTTTGGAAA CCGCTCTCTG CTTTGAGGAT ACGCGGGGAG CTTCCCTGGA 1020 AGCTGTGAAG AGGGGCAGAC ACGAGGCCTC TGGCCAGCCG CGCCTCGGGT CCAGGCCTCC 1080 CTGTGTCCAC ATCTGGTCTC CCGGCTTTTC ACAACAGTGA CCTTGACAGC GCCCAGAGTC 1140 CGCTGCTTCC GTCCAGTCCG CTCTTCCCCT ACGTGGCCAA GAGGACGCAG CACTGGCGGC 1200 TTCAGGAGGT GGCTGTGAGC GCGGGGCTGG GGCCAAGAGC AGAGGACCAG AGAGGAGTCT 1260 CCAAGCCACC ACCGGCCCCG TCACCGGCTA CCGGCTAGGT CAGGCCCCAG ATTCGGGTTT 1320 GCCCAGCGGG CGCTCGGCGT CCACGCTCCC TCTCCACCTT CTTGCCTCTC 1370
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