Tag | Content |
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EnhancerAtlas ID | HS108-00184 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:6577310-6578690 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:6578626-6578647 | AAAAAAAAAGAAAAAGAAAAA | - | 6.09 | IRF9 | MA0653.1 | chr1:6578597-6578612 | AACAAAAGTGAAACT | + | 6.15 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_37180 | chr1:6567553-6581186 | HSMMtube |
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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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Enhancer Sequence | GAGCCGAGAT CGCGCCACTG CACTCCAGCC TGGGTGACAG AGTGAGACTC CATCTCAAAA 60 AAAAAAAAAA AAAAAGATAC AACCAAGCAT ATGCTGAGAA TAGGTGACCA TTCTCTGCTG 120 TTCATGGGGT AGGTATGATA CAGGGGACAC TCCAAAAGGT CTGTAACCCC CAGTGTCACC 180 CACACCTGGA CGCAATCTCC CTTCAGTAAA TAAGCAGGGC CAGGCTTATT TAATTAAGTG 240 GCCATTTTAC TATGTGAGTG CTAGGGGCTC ACATGTCAAC ATGCTGTCGC TGTCACTGTG 300 GCTCACATAA CTCTATATTC CCTGAATACT AGCAGGGGAT GAGCTTGTGG GGGTGAGCAA 360 AGGAAGAAAA AGTCAGCAGC TCAGATTCCT TGCTGGGGAG GGGATGGCCC TGGGAGGAAT 420 TCTCCATGAC TCGCTGTCAG CTTCATAAAT CTGTCGGGCC AGCCATCAGG GAGACAGAGA 480 TAAAGGTTGG AACAGGCTCA GATCTGACGA CAAACAGAAG GGTCCATGGC CCAAATGCCC 540 CGAGGCCAGG CCAGGCCAGG CTATCCCGCT GGGGCCGGGA TGTTTCCCAG ACCAGGCTCC 600 AACTCGGGTA GGAGAATGTT ACTGGATTTC ATGAACGCTA TTCCTGACCC CCGACTCCCA 660 AAATGCGTCA TGGCGGATAT ATATATACAT ATATTTTTTT GAGACAGAGT CTCGCTCTGT 720 CGCCCAGGCT GGAGTGCAGT GGCTCCATCT TGGCTCACTG CAAGCTCCGC CTCCCAGGTT 780 CACACCATTC TCCTGCCTCA GCCTCCCGAG TAGCTGGGAC TACAGGCGCC TGCCACCACG 840 CCCAGCTGAT TTTTTGTATT TTTAGTAGAG ACGGGGTTTC ACCATGTTAG CCAGGATGGT 900 CTTGATCTCC TGACCTTGTG ATCCGCCCGC CTCAGCCTCC CAAAGTGCTG GGATTACAGG 960 TGTGAGCCAC TGCGCCCGGC CGTGTCATGG CGGATATTAA AAGTAAACTT GAAAATATGG 1020 ATGTGCAGGG CCAGACGCGG TGGCTCACGC CTGTAATCCC AGCACTTTGG GAGGCCGAGG 1080 CAGGCAGATC ACCTGAGGTT GGGAGTTCAA GACCAGCCCA ACCAACATGG AGAAACCCCG 1140 TCTCTACTAA AACCACAAAA TGAGCCGGGC TTGATGGCGC ATGCCTGTAA TCCCAGCTAC 1200 TCGGGAGGCT GAGGCAGGAG AATCACTTGA ACCCAGGAGG CGGAGCTTGT GGTGAGCCAT 1260 ATCGCACCAT TGCACTCCAG CCTGGGCAAC AAAAGTGAAA CTCCATCCCA AAAAAAAAAA 1320 AAAAAGAAAA AGAAAAAAGA AAAGAAAATA TGGATGTGCA GGAGGAATTT CCTGGCCCTT 1380
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