Tag | Content |
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EnhancerAtlas ID | HS108-16866 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:40093420-40094800 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr17:40093943-40093958 | TGAACTCCTGACCTC | - | 6.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65441 | chr17:40093840-40095668 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I041938 | chr17 | 40094307 | 40094750 |
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Enhancer Sequence | AGCAATGCTC CTAAGTGCTA TGGTACCCTG GGAGGGAACA ACAGAGATTT GGTCTCCTTT 60 ACCACCATAG TCCCTGAAGG GACATCCCCT TTGCCTTCAA TCCTTACAAT GGGCAAAGGA 120 ATCCAGCGGA TATGTGCTTA AATCCGAGGA TATTAGTTCT AGAATGCTCT GAAACATCAT 180 CTGGTCCAAG TTCTCCTTTT GTAGATAAGG AAATAGAGAC CCTGATTGGG AAGGAACTTT 240 CATAAGTTGA CAAACAAGTT CATGGTGGAG TCAACATCAG AACCCAGGCC TCTGACCTCC 300 AGTCCAGTGC TCTTTCTTTT AAAGACAGAG TCTTGCTCTG TCACACAGGC TGGAGTGCAG 360 TGAAGCAAAT TCGGCTCACT GCCACCTCCA CCTCCTGGGT TAAAGCGATT CTCCTGCCTC 420 AGCCTCCCTA GTAGCTAGGA CTATAGGCGC CCACAACCAC ATCCGGCTAA TTTTTTGTAT 480 TTTTAGCAGA GATGGGGTTT CACCATGTTG GCCAGGCTGG TTTTGAACTC CTGACCTCAA 540 GTGATCTGCC CACCTCGGCC TCCCAAAGTG CTGGGATTAC AGGTGTGAGC CACTACACCT 600 GGCCAGTCCA GTGCTCTTTC CACCACACTG CTGCCAGTGA CAGGATGAAG GACAGAAGCC 660 TGAGATGAAT GTCCCACATC AACATGGGGA TGGGAGTATT GCCATTAGCT GATAAGCCTG 720 AGCAGGGTCA CCTGTGAATC AAATGCCTCT TCTCCAGAAT TGGCTTCCCA AGGTCATGTG 780 TAGGGTTCCC TGTTCTGTGA CACAGGAACA GCTTCACTGC TGGCACATCT CCTTAGCAAC 840 AGGCCTGAAT GCCTCCTATT CTCCAGAGGA CCCGCTGCGG AGGGAAGAGG TGGCTTGAAT 900 ATTACCTCAA GTGGCCTTGT AGCTTTGCTT CTGGCTGTAA CCTCTGGCCA GGCAGTGGGC 960 AGGACTTGGG CACCCGCCTT CCAGCTTCCA GCATGCACAG GCCCACTGGG CACCTGGGAA 1020 ATCACTGGGC ACTGGCAGCC TGGGCCAGAT CGTGCATTTA GACTCAGTGT TATCTGAGGA 1080 CACAGCTTGA ACTGGGGAAG CCCCGAGGCT TCTCAGCGAG CCATCCACCA GCTGCCCCTT 1140 CTGGCTAGCT CCTCATATCT TGCCATAAGG GGCCCATAGC ATGGAACTCC CTGATAGTGG 1200 GGCTCTGGCT GCCTCCTGGC CTGGATAAAC CCACTCTGCC ACTATGCGCA CTCACACTCC 1260 TCTCTGTTTC AACAACTCCA AGCAGAGCAA GTTCACAGAG GGCCCTGCAG CGGCCACCGG 1320 GAGGAAACAG GAGGCAAATC CCTTAGAGGC CTGTTCTCCT TGGCGCCTCC TCACACCCCT 1380
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