Tag | Content |
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EnhancerAtlas ID | HS098-48066 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr6:27655000-27656340 |
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) |
Sox3 | MA0514.1 | chr6:27656244-27656254 | AAAACAAAGG | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr6 | 27655000 | 27655243 | chr6 | 27655152 | 27655475 | chr6 | 27655751 | 27655869 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I027687 | chr6 | 27654780 | 27656741 |
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Enhancer Sequence | GGAAGAGGGG GAAAGTAGAA ACTTGTCAAA AAACAGACAG TAAATCATGA ATTAGCTGCT 60 CCAGTGGCCC CTTCCTGGGT TGTCACCTGC CAGCAAGAGC ATCAGGCTCC GTCTGGAAGC 120 GGGGCACCTC TCAGGGGCAA ATGTTTCACG CCTGCTTCCT CTGAGTTGTC GAATCCGGGC 180 CTCGCCTCCT CCTCCCTTTT CAGATCATAG GATTTCTCTC CCCCGCAAAT AATGGCCCTT 240 ACTTCGTAAA CACGCTGGCT CCGTAATCCC TATTATTGTT TTGGGGGTTT GGTTCTGTCC 300 AGGGAGGAGG TGAGGGCAGA TGCTCAAGAG AGGCTGTCCC CACCGTCCTT TTGTCTCAGC 360 GAACCGCAGT CCGCGCCCGA GCGCCACTAG CTGTCCTGGG ACGGGAACTG CAGCGGCAAG 420 TGTGTGACTT TCTTGAGCCC GGAGCCACAG GCCTGGGAAG CGCCGCTGAG ACTTCAGGGT 480 CGTAGTGACA GAGGAACCAC CCGAGGCTAG GCGGGGAGAG GGTGCAGTTT CCGGATCCCG 540 AAGGCTTCGA GAAGAGCCGA CCTGTCTGGA AGGGTCTCCA AGAACAGAGA GGACTCTGCA 600 ACCATCACTC GGGAGCCGCG TCCTTTCATC CTTGAGACAG CTCCGTGGTC CAACGGTTCC 660 CCGATCCGCT GGCCGAGATC TCAAGCTTGG ATGCAACTTC GGATTCGCCC CAGGCAGGAG 720 GAAGGAAGCC CCGATTGGAA ACGTTGACTT GAATCTTCTC GGATCAGAAT TAGCAGGTTA 780 AGAAAAACTG TTTCCCCGTA AGAAGCAGGG TTCTTTGGTG TTCAATGTGG AGCTCCGCCA 840 CTCCCAGCCC GGGTGAAGGA AAACTGGGAA ACAGAATGAA TGTGATTATC TATTCGAAGA 900 TAAATTTCCA CAAAGCATGC CGTTTGATAG TAGCTTATAA TGTGGAAGTA AGGCATCCTG 960 TCATCCGGCC GGTTAGCTCA GTTGGTTAGA GCGTGGTGCT AATAACGCCA AGGTCGCGGG 1020 TTCGATCCCC GTACTGGCCA AGTATTCTCT GTGGCTTTTA TCACCAGAAT GGATAGTAAC 1080 CCAGACATCG ATCTAAACGT GTACCTGTGT GTTTCTCCAG GCTTAACTTT GCCCCGAGAA 1140 AACGGATCTG TGAATTTGGT GCGCCCTCGC TTACTCGACA GCGGTTAATT TGAACGGGGA 1200 CGTTTCTTTC CGCTGCCTCC AAGGCATACC CACATCCTAC CCGTAAAACA AAGGGGCTAT 1260 AGGCACCTTA CAGTGACAGA GGTACGTTAC GGTTGGAGGC TTTTGTGATT TTTGTCCTCC 1320 TCTGCCCCGG GGAAATTTTC 1340
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