| Tag | Content |
|---|
EnhancerAtlas ID | HS060-33872 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr8:101455250-101455760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr8:101455376-101455397 | TGAGAAGGGTGGGGAGGAGGA | + | 6.8 |
|
| | 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 |
|
| | 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 |
|
Enhancer Sequence | TTCAGACACG ATTCATGGCC TGCCTGATTG CAAGGCCATG GTTCTGAAAA CTTTACTGCC 60
TTTCAGCATC AGTGCCTCTT GCTGAGAGGG GCTGGGGAGG CTGTCTCCGA TAGCTCCTCT 120
GAGCCCTGAG AAGGGTGGGG AGGAGGACGT GAGACAAGGG ATAGGGAGCT AGTGGCTCTG 180
GCAGTGGCAG AGAGTTGTTC GGGAGAACTT CGGTGGTGGT GGAGGCGGTG AGGATGCTCA 240
GAGCTCATTT GTATGTGTGA ATCATTTGTA AGTTGAGGAT TAGTCAGAGG TTGGCTGCAT 300
TGTTACGGAA ATAGTGGGCT GGGTGTGTGC TCAACCTGAA GCTGTGAGGG CTGAATTTTT 360
TCTCTCCTGG AGACATTGTG AACCACAGAA GGCAAGTCAG CTTTTGGGGG CGAGTTTTAA 420
GTGGAGAAAT ATCTCCTTCT CTAATGCTTG CAGTTGGCTC TGAGGGTTGT GGAAGAAAGA 480
CACAATTTAG AGAACTTATA ACGTCCTTGG 510
|
