Tag | Content |
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EnhancerAtlas ID | HS108-08925 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr12:6362090-6363510 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYC | MA0147.3 | chr12:6362281-6362293 | GAGCACGTGGCC | - | 6.92 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 6362600 | 6362825 | chr12 | 6362472 | 6362600 |
| | Number: 1 | ID | Chromosome | Start | End |
GH12I006253 | chr12 | 6362561 | 6362710 |
| Enhancer Sequence | CTCTCAAAAA AAAGAAAAGA ATATGAAAGA AAAGAATTCC CACAGAAGAC ATCTTACATC 60 CTGTTGGCCA GATATGATCA CATGCCCATT CTTAAACCAG GCAAGTAGGG TGGGAGGAAT 120 TACCACGGCA GGTCAGGCAA AGCAGTACTC ATTCCCCAAC ACCCAGGGTT GGGAGGGTCC 180 TGCCTCACCT GGAGCACGTG GCCTCCAGAC ACCCGGAGTC AAGTGGGACA CAGCAATTTA 240 GTGGCCCTAA CACTGTGAGC CAGACTCATC TATCCCCCAC ATTGTACTTT CATCATCTCA 300 ACCTGTGAAA GGTATAAACT GCTGGGCAGG AGATCTGTAT TTTGAAGATT TTATAGGGAG 360 AGGGTTGGAG AGAGAGTGAT ATTTTACCAG ACACTAAAAC CTTCAAGAAA TGATGGGGAG 420 TGACCCAGGA GTCAGTAAAT AATTGCAACA AGGTGATTCT TACTTCGTGC TCCAAGACGT 480 CTGTTCTTTC CTGCTTTGTG ACGCAGGCCT CCGTGCTGGC ATTTGTGAAA TGCAGATAAC 540 CTGTCTAATC TCTAAGGTCT CCAGTACTCT GGTTGTAATC TCCTGAGGCC AGGAGCTGGG 600 TCTTCAGGTC TTCACTTTCT CTCTATGTCC CCAACACAGC TCTGGGGGCA GGGTTGACAT 660 GCAGTGTGGA CAGTAGCCAT TCAAGAATTT TAACATTTTC AGGCCGGGTA CAGTGGCTCA 720 TGCCCATGAT CCCAACACTT TGGGAGGCCG AGGCAGGCAG ATCATGCGGT CAAGAATTCG 780 AGACCAGTCT GGCCAACGTG GTGAAACCCC GTCTCTACTA AGAAAATACA AAAATTAGCT 840 GGGCATAATC CCAGCTAATT CGGGAGGCTG AGGCAGGAGA ATTGCTTGAA CCCAGAAGGT 900 GGAGGTTGCA GTGGGCCGAG ATCGTGTCAC TACACTCCAG CCTGGGCAAC AGAGCAAGAC 960 TCCATCTTGG GGGAAAAAAA AAAGAATTTT AACATTTTCA ACTCTGTGAG AGACCCCATT 1020 CTTCATGAAA TGGAGTGATT CGTAGCTGTT ATCGAAGCGT GAAATCTGAA TTTCATGCTG 1080 TGAGAATCTG CAAGAGTGAC TCAGATAACT GGTGAGGGAG GCTGTGGGGT ACATTGCAAA 1140 GGCCTTGTAG GGAGGGAGAC AGACTTGAGA TCAAATCCTG GCTCTGACAC TTACTGAGTG 1200 ATCTTGGACA AATCACTTAA CCTCTAAACT CCTGGCTCTC CTCTATAAAA TGAAGGGCAG 1260 GCTGGGCACA GTGGCTCACG CCTGTAATCC CAGCACTGGG AAGCCGAGGC GGGTGGATCA 1320 CTTGAGGTCA GGAGTTCGAG ACCAGCCTGA CCCCATGGTG AAACCCCAAC TCTACTAAAA 1380 ATACAAAATT AGCCAGGCAT GGTGGCAGCC ACCTGTAATC 1420
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