Tag | Content |
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EnhancerAtlas ID | HS133-05899 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr11:65662870-65664270 |
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) |
EWSR1-FLI1 | MA0149.1 | chr11:65664012-65664030 | CTTTCCTTCCTCTCTGCC | - | 6.34 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_40472 | chr11:65663663-65664738 | K562 | SE_44975 | chr11:65662742-65671764 | NHLF | SE_47245 | chr11:65653835-65672695 | Panc1 | SE_56176 | chr11:65662492-65672275 | u87 | SE_64549 | chr11:65662910-65664927 | NHEK | SE_67476 | chr11:65662492-65672275 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 65663074 | 65663440 | chr11 | 65662976 | 65663055 |
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Enhancer Sequence | AGGCGTGAGC CACCATGCCT GGCCTTAAAC TAGATTCTTA ACGCAACTTT CCATGAAAAA 60 CTGAAGCCCA GAGAGGATAA CTTACTTATG GTTCCAGAGC AGGACTTAGA ACCCATAGAA 120 CTCACTCACT CTATTCCACA TTGAGTGACA GGCCAGATGA GAGAGACCAT TTCACCAAAA 180 GGATCCAACT CACAGCTCAC AGCCCTACCT GGAGAACCCA GGATCAAAGG GTCACCCTCA 240 GGACCAGGCT GAAGGAAGGA CGCACAGGAG GGTTTACCCC TGGCCCGCTT CTGCGGCTCA 300 TACCACAGTC CCTCCTCACC ACAAAGGCCA GACATTCTGT TCTGGGAAAC CTGTCTCTGG 360 CTGATCTCTC ACCTTTCCCA GGGCCCTAAC CTCTCTCCCC ATCCTCTACC TGCCGACCAA 420 GCTTTTTAAC CTCATCCCCT GTAGTCTCCC ACACCAAAAT GCCCCAGGGA GAGGAAAGAT 480 GAGCCACTCC TTTAAAGACT CGCCATCTCT TACTCACTTA TTTTGGTAAG GGCTTTGGGG 540 AGCCAAGAAT TGTCAGTTCC CTCTACTTTG AGCCTTCTGT TAGCTTCCAG TGAGACAGCG 600 TGGCTTGGTG ATTAGTTTTG GGGGTTTTAT TTTATTTTGT TTTTTCGGTA GAGACAGGGT 660 CTCTCTATGT TGCCCAACCT AGTCTTGAAC TCCTGGCCTC AAGTGATCCT CCTGCCTAGG 720 TCTCTCAAAG TGCTGGGATT ACAGGCATGA GCTACTGCAC CTGGCCCTGG TTTGGTGGTT 780 AGGATCTGAC TTTAGAGTTG TATAGACCTG GGGCCAAGGC CAGTCCTGTG TCATTACTCA 840 CTACTTGTGT GATCTTGGGC AAGTGACTAC CCTTCTGTGC CTTCATTTCT TTGGTGGAAG 900 ATGGGGAAAA CCAGAGTACA TTCCCCAGAG AGATTTTGTG AGGATTAAAT GAGACAGGGA 960 AACTGAGACT GAGGGAGTAG CTGAAGGGAA CCCTCTTGTT CCTGTTCTCT CCCAGACAAC 1020 ATAAGCGCCC CCTCTATGCA TGTCAGCAGG TGGAGACCCC CTCACCATTC CGTGTGCGCA 1080 CCTTACATGT TCTTGCCTCC GCCTCCATCC TTGCTCCTGC CACCCCCGCT ACCTGGAATG 1140 TCCTTTCCTT CCTCTCTGCC TCTGCCAGTC CTACCCATCC TTCTAGGCTA ATATGCCACC 1200 TTTTCCAGGA AGCTTTCCCT GATCTGGAAG TGACTGTTGT ACCCTCTGGG CCTCCCGTGG 1260 GGCTCCTATC ACTTTCAGCC TTGGGCAGTA GTCACCTGTA GCCTACCTTA CCCCCTCCTA 1320 AGCCTGTGCT CTCCTTTCTG GCAGGAGCTT CTCTGCACCC TAGCACTCCT GGGCGGGGTC 1380 GGAACCACTG CAATGCCTCT 1400
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