Tag | Content |
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EnhancerAtlas ID | HS093-12267 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr16:89506930-89507550 |
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) |
ZNF263 | MA0528.1 | chr16:89507034-89507055 | GGAGGAGGTAAGAGGGAAAGG | + | 6.39 | ZNF263 | MA0528.1 | chr16:89507028-89507049 | GGGGGAGGAGGAGGTAAGAGG | + | 6.87 | ZNF263 | MA0528.1 | chr16:89507031-89507052 | GGAGGAGGAGGTAAGAGGGAA | + | 7.11 | ZNF263 | MA0528.1 | chr16:89507022-89507043 | AAAGGAGGGGGAGGAGGAGGT | + | 7.7 | Zfx | MA0146.2 | chr16:89507405-89507419 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_09347 | chr16:89505663-89508004 | CD14 | SE_18507 | chr16:89506051-89507763 | CD4p_CD25-_Il17-_PMAstim_Th | SE_45841 | chr16:89505714-89507531 | Osteoblasts |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH16I089440 | chr16 | 89506410 | 89512171 |
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Enhancer Sequence | GGAGAATTGC TTGAGACCAG GAGGTCAACA CTACAGTGAG CTGTGAGTAC CAATGCACTC 60 CAACCTGGAT GACACGACAA AACTCTGTCT CAAAAGGAGG GGGAGGAGGA GGTAAGAGGG 120 AAAGGAAGAA AGCATAAGAA AATATCAAGC ACAAACTAAG GGCCCCAAAA AATCCAACTC 180 ACAGCAACGT GGGCAGAGCC CTGGAGAAGC CAGAGGACAT CCAGGCACCA CCCAGCAAGG 240 GGCTACAGAA AGGGGGCCAC CTGCCTCCAA GCCTGCCGGG ACTGAAAATA AATCCATGTG 300 GCATCAACAG GAACATCTGT GGCTGTGTGG CAATGCGTGT GAGTGCGCAT GAATCCTGGT 360 GTGGCTGGTG TGTGTCACAG TCAAAACGGA AAGAGAGAGC GCATCGTGGT TTATAAAAAA 420 TAAGTTTCCT TGCGGCCAGA CACAGTGGCT CACGCCTGTA ATCCCAGCAC TTTGGGAGGC 480 CGAGGCGGGC AGATCATGAG GTCAGGAGAT CGAGACCATC CTGGCTAACA CCGTGAAACC 540 CTGTCTCTAC TAAAAATACA AAAATTAGCC GGGCGTGGTG GTGGGCGCCT GTAGTCCCAG 600 CTACTCGGGA GGCTGAGGCA 620
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