Tag | Content |
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EnhancerAtlas ID | HS146-02828 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr11:65662860-65664270 |
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 | CTGGGATTAC AGGCGTGAGC CACCATGCCT GGCCTTAAAC TAGATTCTTA ACGCAACTTT 60 CCATGAAAAA CTGAAGCCCA GAGAGGATAA CTTACTTATG GTTCCAGAGC AGGACTTAGA 120 ACCCATAGAA CTCACTCACT CTATTCCACA TTGAGTGACA GGCCAGATGA GAGAGACCAT 180 TTCACCAAAA GGATCCAACT CACAGCTCAC AGCCCTACCT GGAGAACCCA GGATCAAAGG 240 GTCACCCTCA GGACCAGGCT GAAGGAAGGA CGCACAGGAG GGTTTACCCC TGGCCCGCTT 300 CTGCGGCTCA TACCACAGTC CCTCCTCACC ACAAAGGCCA GACATTCTGT TCTGGGAAAC 360 CTGTCTCTGG CTGATCTCTC ACCTTTCCCA GGGCCCTAAC CTCTCTCCCC ATCCTCTACC 420 TGCCGACCAA GCTTTTTAAC CTCATCCCCT GTAGTCTCCC ACACCAAAAT GCCCCAGGGA 480 GAGGAAAGAT GAGCCACTCC TTTAAAGACT CGCCATCTCT TACTCACTTA TTTTGGTAAG 540 GGCTTTGGGG AGCCAAGAAT TGTCAGTTCC CTCTACTTTG AGCCTTCTGT TAGCTTCCAG 600 TGAGACAGCG TGGCTTGGTG ATTAGTTTTG GGGGTTTTAT TTTATTTTGT TTTTTCGGTA 660 GAGACAGGGT CTCTCTATGT TGCCCAACCT AGTCTTGAAC TCCTGGCCTC AAGTGATCCT 720 CCTGCCTAGG TCTCTCAAAG TGCTGGGATT ACAGGCATGA GCTACTGCAC CTGGCCCTGG 780 TTTGGTGGTT AGGATCTGAC TTTAGAGTTG TATAGACCTG GGGCCAAGGC CAGTCCTGTG 840 TCATTACTCA CTACTTGTGT GATCTTGGGC AAGTGACTAC CCTTCTGTGC CTTCATTTCT 900 TTGGTGGAAG ATGGGGAAAA CCAGAGTACA TTCCCCAGAG AGATTTTGTG AGGATTAAAT 960 GAGACAGGGA AACTGAGACT GAGGGAGTAG CTGAAGGGAA CCCTCTTGTT CCTGTTCTCT 1020 CCCAGACAAC ATAAGCGCCC CCTCTATGCA TGTCAGCAGG TGGAGACCCC CTCACCATTC 1080 CGTGTGCGCA CCTTACATGT TCTTGCCTCC GCCTCCATCC TTGCTCCTGC CACCCCCGCT 1140 ACCTGGAATG TCCTTTCCTT CCTCTCTGCC TCTGCCAGTC CTACCCATCC TTCTAGGCTA 1200 ATATGCCACC TTTTCCAGGA AGCTTTCCCT GATCTGGAAG TGACTGTTGT ACCCTCTGGG 1260 CCTCCCGTGG GGCTCCTATC ACTTTCAGCC TTGGGCAGTA GTCACCTGTA GCCTACCTTA 1320 CCCCCTCCTA AGCCTGTGCT CTCCTTTCTG GCAGGAGCTT CTCTGCACCC TAGCACTCCT 1380 GGGCGGGGTC GGAACCACTG CAATGCCTCT 1410
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