| Tag | Content |
|---|
EnhancerAtlas ID | HS098-39661 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:119513910-119514500 |
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 | ACACCAGATG AAATTGCTCT TCCAAACACC ACTAGCTGGG GAGTTGGCTC TTGGCTGGGG 60
TTGGTCAGTG CACAGGCCAG TAAGGGAGCT GGGCAAGTGC AGAAGTGGAG ACTAGCTGTG 120
TCCCAGACAG CGACTCTCCG GCTGTGACCC TGGAGAGTCC TTTAGCAGGG CAAAGTGCAA 180
CATAGGCAGA CCTTAAGGGA TGACTCAGTA ACAGATAAGC TTTGTGTGCC TGCAGGGGGA 240
TGGGAAGAGG GTGGGGCAGG AGAGGGACAT AAAAGGGCTC TGAGGCATTG TACTGTGAAT 300
TCCTTCAGTC TCCTGCTCTG CTCAGCCAGT CAGCCCTGCC TCCCTTGTTT AGGACCACAC 360
AGCACTGCTG GGTGTCTGCC TTTCCTTGTG ACTCTTCTCT AGCCTCTGCA TGGCCAGCAG 420
CCCTCTTCTT TTCTCCTATT CTCTTAAGAA ACATGCCCAT CACCTGCAGT TTCTCTGGGC 480
TCCCCGTTAA TCTGCCTTCC TCATCTCCTA ATGCTGCCTC CTCCCTCCCA TTGCCGGTGC 540
CTGGAAATAG TCAAGGCTGG GTTCTGTTCT TTTGCTTGAA TTTCTTTCAC 590
|
