Tag | Content |
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EnhancerAtlas ID | HS060-13764 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr16:89505770-89507510 |
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: 2 | Chromosome | Start | End |
chr16 | 89506936 | 89507394 | chr16 | 89506328 | 89506577 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I089440 | chr16 | 89506410 | 89512171 |
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Enhancer Sequence | TTCCTTGACT TGCAATGGGG TTACCTCCCA ATAAACCCAG TGTAAAGTCA AAAATCCTAA 60 GTCGAACCAT CATTAAGTCA GGGACTATCT GTATACACTT TCAGTGCTAA AAACTACACC 120 AAAGAAAAAA CAAGTGTCAA AGTTCTCCAT GTAAAACAGT GATCCAGGGA TATGGGTGAG 180 AAAACCCATC TAAAATGCAA TGTGATATTT AGGATAAAGC TGAAACACAC CACAGCGCCT 240 CAGCAATTGA GGCTGTGAAT ACAACCACAC AATCAGCAAA GAAAAGCTTG TTCTATTCTT 300 CATCTACACC ACTCACACAC AACACCAAAG GTGTTCTCAG CACACCTCCA TCCACCTCAG 360 ATCTATTCTT CATCTACACC ACTGACACAC AACACCAAAG GTGTTCTCAA CACAACTCCG 420 TCCCCCTCAG AACTCTGTGG AACGTTTTCA TTCCCAATGA TCACCAACAG AGCCAGCTGT 480 AAGCTCAACT CTAACACTAC CCACAGTGCA GCTGACCTAG ACTGATGGGC GGCCTCCGGA 540 GAAGTCAAAG ACTCCAGCTC TACTGCACAC ACCCACAGCA GGAGAGGCCT GTGTCTCTCA 600 CAGGTGTGGG GTCTGAGCCG CAGCCCACTA CCTTAACTCC ATAATCTGTG ACTTGGCTCT 660 TATGAGGAAG CTGACAAAGA ATCAGAGACT CAGAGGAGAT CACAGCCTTT CAGGACTGAG 720 GTCTAAAACA CAGAACCTCT AGCCCAGTGC TCACCCGCAA CCATTTCCCT GCCTCTTCCT 780 ACTTCTCCAG TCCTCAAGGG GACAATGGCA GGGTTCACAG GATTCTTCCT CCGGAAGAAT 840 TCAGTGTGCT GTAATTAGAA ATGAACATTT TATCAATATG TTCACGTAAA ATGTACATGT 900 TCCCCTGGGG GGAGGGATAA ATAACAGTGG AACTAGGAAA AGCAGACCAC CAGAAAATGT 960 CTCGGTCCAG CGTGGTGGCT CAGGCCTGTA ATCCCAGAAC TCTGGAAGGC TGAGGGGGGA 1020 GGATCACATG AGGCCAGAAG TTCAGACCAG CCTGAGCAAC ACACTGAAAC CTCAACTTTG 1080 TAACAATAAA AACAGAATAA AAACTTAGCT GGGCATGGAG GTGTGCACCT GTAGTCCCAG 1140 GCACTCAGGA GGCTGAGGTG GGAGAATTGC TTGAGACCAG GAGGTCAACA CTACAGTGAG 1200 CTGTGAGTAC CAATGCACTC CAACCTGGAT GACACGACAA AACTCTGTCT CAAAAGGAGG 1260 GGGAGGAGGA GGTAAGAGGG AAAGGAAGAA AGCATAAGAA AATATCAAGC ACAAACTAAG 1320 GGCCCCAAAA AATCCAACTC ACAGCAACGT GGGCAGAGCC CTGGAGAAGC CAGAGGACAT 1380 CCAGGCACCA CCCAGCAAGG GGCTACAGAA AGGGGGCCAC CTGCCTCCAA GCCTGCCGGG 1440 ACTGAAAATA AATCCATGTG GCATCAACAG GAACATCTGT GGCTGTGTGG CAATGCGTGT 1500 GAGTGCGCAT GAATCCTGGT GTGGCTGGTG TGTGTCACAG TCAAAACGGA AAGAGAGAGC 1560 GCATCGTGGT TTATAAAAAA TAAGTTTCCT TGCGGCCAGA CACAGTGGCT CACGCCTGTA 1620 ATCCCAGCAC TTTGGGAGGC CGAGGCGGGC AGATCATGAG GTCAGGAGAT CGAGACCATC 1680 CTGGCTAACA CCGTGAAACC CTGTCTCTAC TAAAAATACA AAAATTAGCC GGGCGTGGTG 1740
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