Tag | Content |
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EnhancerAtlas ID | HS184-29254 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr8:41486370-41488860 |
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) |
Gfi1b | MA0483.1 | chr8:41486812-41486823 | AGCTGTGATTT | - | 6.14 | ONECUT1 | MA0679.1 | chr8:41488263-41488277 | AGTATTGATTTTCT | - | 6.48 | ONECUT2 | MA0756.1 | chr8:41488263-41488277 | AGTATTGATTTTCT | - | 6.28 | ONECUT3 | MA0757.1 | chr8:41488263-41488277 | AGTATTGATTTTCT | - | 6.45 | TFAP2A | MA0003.3 | chr8:41488408-41488419 | TGCCTCAGGCA | + | 6.02 | ZNF263 | MA0528.1 | chr8:41488015-41488036 | TCCTCCCCTCCTCCATGCTTC | - | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 41486785 | 41486865 | chr8 | 41487950 | 41488822 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I041630 | chr8 | 41488261 | 41488410 |
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Enhancer Sequence | GTTGAACTCC TGGCCTCAAG CAATCTTCCT TTCTTGGCCT CCCAAAGTGC TGGGATTACA 60 GGTGTGACAC ACCTTGCCCA GGTGACGAAA ATGCACTTTC AGTGCATTTG AACCCCTCCA 120 TATGCACAGA CTCAGCTCTG GATGGCTGGA TGTGAGATCA AGAGGTTAAC TGGTGCCTTT 180 CCTTCTGATT CATCCAGAGT CCTAGGCAGA TGTTCGGAGG CTCCCTCTGC ACCCTCTTGC 240 CCTGTGTTCC AAATACAGAC AAACACCTTG CTCCTCCCTG CTGAGGAGTC AGGGCTGGGT 300 GGGGGGCACG GAGGCCCTGC TCAGCCTCTG CAGGAGAGGC TGGAAAGAGA GGCTGGGAGG 360 GCCCAGCCTG GGGCCGGGGT CCCGGTTCCT GCTGCTCGGC GTGGGCTTGG GGAAGGGCTG 420 TGCATACGCA GATTGATCCG CCAGCTGTGA TTTGTCATTT CTCCCAGGCA GGCGCTGTTT 480 TCTCTTGGTT CAGGAGGCCC CTTCGACACC TGCTTTATTT TTCTTCCTGC GCTGACGTGA 540 CGGGAGACAG GTGTTAAACT ACTTAATCAC TTTAAAATTG TTTTAATTTT CTGTTTTTTA 600 TTGATCTCTC CAGCACCAAT TAATCAGCTC ACTGGACCAG GCAGTTAGTA CATTAAAAAT 660 TGTCAGGGAG GCCGTGCATC TTGCAAAATG TCTAAAAAAT ATTCGGCTGG CAAATTTTGC 720 TTTTCTTTGG CATGCAACAG TCCGTGGCCC ATGAAACTCC CACTCAGAAA AGGCCTCTGC 780 CTCCGGGACT CGTGTGCAGG GAGTATTCAG GCCACTGCAG GAGCTCTGGC CAGGGGCTTC 840 TGGTAGGGCA ACACTGGACG CAGGTGCCTG GCTCATCAGT GATTTGCCAC CTTTCCTTCC 900 ACTTTTGTTC TGTTTCTTAC ACATCCTGGG TCTGATTTCC CCAAGGACTT TGGGAGTTTT 960 TGTGGAAGGG GACTTGACAG TCTGTAACTG CCCCGTGAGG CCAGGACAGA GGGTCTAAAG 1020 CAACTGTCCA TTTCCACAAA ATCTCCCAAC ATCCGGCCCC TGAGCCCACA GCCAGATTTC 1080 CCCTCCCTGG GACATGAGCA CTTTTGACTT GTCCTTCTGA CAATGCCAAA ACCACCTCCC 1140 TGGGGCAGGG GACCCCTATG CTGGGTACAC TCCGTCTGCT GGCGGGCAGC GGTTGTGTCA 1200 TGCTGCCTCT TCCCCGGCAC CCAGTGATGG GCCTGAAGCC CTTCCACAGA ATGTCCTGGG 1260 CAGCGCCACT CCACACCCAC TGTCACTGTC ACTGGCTCCT GTGCTGCAAG CCTTCACTGC 1320 CTGTCTTTTG TCACCCCTCT GGAAAATGAT TTATTAACTA CTTGGCTGTA CTTCTCATTC 1380 AATAAAATAT GGATGGAACA ACCAGAGACT TCAACCTCAC TTCTTGGGGT GAGAACTGTG 1440 TTTTCCAGTT TTCCCATGTT CGCCTAGTTT CCTATGACTT TCCAAGAGCA AGCCTCTTAT 1500 TTCTTCTGGG GTGCTTTAAC CATCCCGCAG ACTGTCCGCA GGGTCTGGGT CACCCGCTTC 1560 TTCCTGGGAG CACCACCCTC CCACAGCAGC CCTTGTTCCC CTACCCCTGT CTGCAGGCCC 1620 AGTGGGCCCC GTGCAGATGG ACATTTCCTC CCCTCCTCCA TGCTTCCGGC TCACGGGGCT 1680 CCGCAGAGAG CTAAGCCCAG GCCCTTGAGA CTCAGGGGTC CCAGTCCCTA CTGAGAAGGG 1740 CTGCCCCCGG CCCCCCACCC CACATTCTGG AAAGTTGGAG GGCGTGGGCC TCGGGGGCCG 1800 GCACAGCCAG CCCTGGTTCT GGCCATGGAC TTATCTCCCT CACCCCACCC TCTGGTATTA 1860 ATTGGTATAT GATTGGGCCG GGACATATAA TCTAGTATTG ATTTTCTCTC TGGACGCCAC 1920 AGTTTTATTT GCTCACATCT GCCTTGTGTT TAATTGGTGC TTTGCTCTGG AAACAGAGAT 1980 CTTATCGGCC TGCTGGGTTT CTTTTCCTGG GGCACACAGG CACGCACAGT CCCAACCCTG 2040 CCTCAGGCAC GCACAGTCCC AACCCTGCCT CTCCCGGACC CTCCCACAGC CAGGCCTGCC 2100 CAGGCTTAAG GGGATGGCGG GGAATGACCC AGGGGGTTTG CTTTACTCTT GACCTCCCGA 2160 GCTGGGGCTG ATCCTTCCTG GAGTGAATGT GTGTGTGTCT GCGATGATCA CTGGGGAACG 2220 CTGGCTTTGG GTGGGGCCTG GGTTCATACC CGCTTCCTCC ATGTATGTCT TCGCGGCTGG 2280 CATCTTGAGT TTTTCGGCAC AGTAATATCT CTTCCTTATC TGAGAGAAAG GTAGAATGGA 2340 TACCTGCTCT GTAGGACTCC TGGAGATTAC CTTTCAGGCC CCATACAGCA CCTGGCACTT 2400 AGTAGGCGTA ATGAACAGCA GCTCCTTTGT CACTTGCCTG GTCCCACTCA GCCCATGCAG 2460 CTCTGTCAGA GGCCTGTGAA CCAGAGCAAC 2490
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