| Tag | Content |
|---|
EnhancerAtlas ID | HS050-48326 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr3:119513840-119514480 |
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 | AATTGTGTAA GCCTCAGAAC CCACGTAAGC TGACTAAAGG GCACCTCTAC TTGCCCATTG 60
ACTAACCTGA ACACCAGATG AAATTGCTCT TCCAAACACC ACTAGCTGGG GAGTTGGCTC 120
TTGGCTGGGG TTGGTCAGTG CACAGGCCAG TAAGGGAGCT GGGCAAGTGC AGAAGTGGAG 180
ACTAGCTGTG TCCCAGACAG CGACTCTCCG GCTGTGACCC TGGAGAGTCC TTTAGCAGGG 240
CAAAGTGCAA CATAGGCAGA CCTTAAGGGA TGACTCAGTA ACAGATAAGC TTTGTGTGCC 300
TGCAGGGGGA TGGGAAGAGG GTGGGGCAGG AGAGGGACAT AAAAGGGCTC TGAGGCATTG 360
TACTGTGAAT TCCTTCAGTC TCCTGCTCTG CTCAGCCAGT CAGCCCTGCC TCCCTTGTTT 420
AGGACCACAC AGCACTGCTG GGTGTCTGCC TTTCCTTGTG ACTCTTCTCT AGCCTCTGCA 480
TGGCCAGCAG CCCTCTTCTT TTCTCCTATT CTCTTAAGAA ACATGCCCAT CACCTGCAGT 540
TTCTCTGGGC TCCCCGTTAA TCTGCCTTCC TCATCTCCTA ATGCTGCCTC CTCCCTCCCA 600
TTGCCGGTGC CTGGAAATAG TCAAGGCTGG GTTCTGTTCT 640
|
