| Tag | Content |
|---|
EnhancerAtlas ID | HS047-24324 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr3:119513780-119514610 |
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 | TGTCTCAAAA TAAGTAAATT AAATTAAATA ATGTAAAATA AAATAAAATA GGACTGCCCA 60
AATTGTGTAA GCCTCAGAAC CCACGTAAGC TGACTAAAGG GCACCTCTAC TTGCCCATTG 120
ACTAACCTGA ACACCAGATG AAATTGCTCT TCCAAACACC ACTAGCTGGG GAGTTGGCTC 180
TTGGCTGGGG TTGGTCAGTG CACAGGCCAG TAAGGGAGCT GGGCAAGTGC AGAAGTGGAG 240
ACTAGCTGTG TCCCAGACAG CGACTCTCCG GCTGTGACCC TGGAGAGTCC TTTAGCAGGG 300
CAAAGTGCAA CATAGGCAGA CCTTAAGGGA TGACTCAGTA ACAGATAAGC TTTGTGTGCC 360
TGCAGGGGGA TGGGAAGAGG GTGGGGCAGG AGAGGGACAT AAAAGGGCTC TGAGGCATTG 420
TACTGTGAAT TCCTTCAGTC TCCTGCTCTG CTCAGCCAGT CAGCCCTGCC TCCCTTGTTT 480
AGGACCACAC AGCACTGCTG GGTGTCTGCC TTTCCTTGTG ACTCTTCTCT AGCCTCTGCA 540
TGGCCAGCAG CCCTCTTCTT TTCTCCTATT CTCTTAAGAA ACATGCCCAT CACCTGCAGT 600
TTCTCTGGGC TCCCCGTTAA TCTGCCTTCC TCATCTCCTA ATGCTGCCTC CTCCCTCCCA 660
TTGCCGGTGC CTGGAAATAG TCAAGGCTGG GTTCTGTTCT TTTGCTTGAA TTTCTTTCAC 720
TTGGCTTCTT GACTCTTTCT AAACTACAAT CCCCCCATTC TCACTGCCTT AGTTTTCCCT 780
CTCTCTGTGT TTCTCAAACT ATATCCCACC ACGCCCTGAC AAGGGCTTCT 830
|
