Tag | Content |
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EnhancerAtlas ID | HS098-55619 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr8:101455110-101455790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr8:101455376-101455397 | TGAGAAGGGTGGGGAGGAGGA | + | 6.8 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_18537 | chr8:101453463-101457190 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19357 | chr8:101453387-101456992 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22743 | chr8:101452080-101458132 | CD8_primiary | SE_27991 | chr8:101454826-101458796 | Fetal_Intestine | SE_28830 | chr8:101454704-101458694 | Fetal_Intestine_Large | SE_32305 | chr8:101455108-101456074 | Gastric | SE_32533 | chr8:101454102-101459783 | GM12878 | SE_36367 | chr8:101454853-101457864 | HMEC | SE_62291 | chr8:101421434-101542088 | Tonsil |
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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 |
GH08I100441 | chr8 | 101453434 | 101458655 |
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Enhancer Sequence | TTTATATGTC TTATGTTATT CAATCCTCAC AATTCCCCAA GGGATTAGTA TGGTTGTCTT 60 CCCATTTTAC AGATGAGAAA AACAAGGGTT AGAGAAATTA ATGAACTTGT CTGGCGCCAT 120 GTAGCCAATA AGTGAAGGAA TTCAGACACG ATTCATGGCC TGCCTGATTG CAAGGCCATG 180 GTTCTGAAAA CTTTACTGCC TTTCAGCATC AGTGCCTCTT GCTGAGAGGG GCTGGGGAGG 240 CTGTCTCCGA TAGCTCCTCT GAGCCCTGAG AAGGGTGGGG AGGAGGACGT GAGACAAGGG 300 ATAGGGAGCT AGTGGCTCTG GCAGTGGCAG AGAGTTGTTC GGGAGAACTT CGGTGGTGGT 360 GGAGGCGGTG AGGATGCTCA GAGCTCATTT GTATGTGTGA ATCATTTGTA AGTTGAGGAT 420 TAGTCAGAGG TTGGCTGCAT TGTTACGGAA ATAGTGGGCT GGGTGTGTGC TCAACCTGAA 480 GCTGTGAGGG CTGAATTTTT TCTCTCCTGG AGACATTGTG AACCACAGAA GGCAAGTCAG 540 CTTTTGGGGG CGAGTTTTAA GTGGAGAAAT ATCTCCTTCT CTAATGCTTG CAGTTGGCTC 600 TGAGGGTTGT GGAAGAAAGA CACAATTTAG AGAACTTATA ACGTCCTTGG CCAGATATGC 660 CCAAAGCCAG GATGTCCCCC 680
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