| Tag | Content |
|---|
EnhancerAtlas ID | HS081-13605 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr3:119513860-119514450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr3:119514107-119514118 | GGATGACTCAG | + | 6.32 | | JUN(var.2) | MA0489.1 | chr3:119514104-119514118 | AAGGGATGACTCAG | + | 6.33 | | JUNB | MA0490.1 | chr3:119514107-119514118 | GGATGACTCAG | + | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28530 | chr3:119513306-119516847 | Fetal_Intestine | | SE_29517 | chr3:119513320-119516900 | Fetal_Intestine_Large |
|
| | 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 |
| GH03I119794 | chr3 | 119513178 | 119516613 |
|
Enhancer Sequence | CCACGTAAGC TGACTAAAGG GCACCTCTAC TTGCCCATTG ACTAACCTGA ACACCAGATG 60
AAATTGCTCT TCCAAACACC ACTAGCTGGG GAGTTGGCTC TTGGCTGGGG TTGGTCAGTG 120
CACAGGCCAG TAAGGGAGCT GGGCAAGTGC AGAAGTGGAG ACTAGCTGTG TCCCAGACAG 180
CGACTCTCCG GCTGTGACCC TGGAGAGTCC TTTAGCAGGG CAAAGTGCAA CATAGGCAGA 240
CCTTAAGGGA TGACTCAGTA ACAGATAAGC TTTGTGTGCC TGCAGGGGGA TGGGAAGAGG 300
GTGGGGCAGG AGAGGGACAT AAAAGGGCTC TGAGGCATTG TACTGTGAAT TCCTTCAGTC 360
TCCTGCTCTG CTCAGCCAGT CAGCCCTGCC TCCCTTGTTT AGGACCACAC AGCACTGCTG 420
GGTGTCTGCC TTTCCTTGTG ACTCTTCTCT AGCCTCTGCA TGGCCAGCAG CCCTCTTCTT 480
TTCTCCTATT CTCTTAAGAA ACATGCCCAT CACCTGCAGT TTCTCTGGGC TCCCCGTTAA 540
TCTGCCTTCC TCATCTCCTA ATGCTGCCTC CTCCCTCCCA TTGCCGGTGC 590
|
