| Tag | Content |
|---|
EnhancerAtlas ID | HS050-48566 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr3:126690660-126691520 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr3:126690898-126690911 | TGCAGCTGCTCCC | + | 6 | | STAT3 | MA0144.2 | chr3:126690946-126690957 | CTTCCCAGAAG | - | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_61225 | chr3:126659718-126703478 | HBL1 |
|
| | 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 |
| GH03I126971 | chr3 | 126690205 | 126691470 |
|
Enhancer Sequence | CTGCCCTGCT GCCCCCTCCT CAGTGGGCCT GCGTCCCTGG GGCTGGTACC TGGCACACCA 60
CGTGCCCAGG AAGGGTGGGC AACTCGGTTG GCCTGGGCTT CTGAGGGCAC AGGAGAGCTG 120
GGCTGGTTCT GCCTGCGCAT TTTCTGTGGA ATGCAGACCA TGCTGGCAAC ACCAGGGCCT 180
CGGGACACCT CTGCTTCTGA CGCAGGCCCA GGACAAGGGG TGATGCCCTG TGGTGAGCTG 240
CAGCTGCTCC CAACCCAGGC CGGGTGGGCG GGTGCTTCAA GGCAGGCTTC CCAGAAGAGG 300
AGGAGCCTGT GCGGGGGCTG GAGGAAGGTC AGCAGGGTGA CCTCAGGGGA AATAAGTTGT 360
TCCCTCTGTC TCCAGAACAG AGGAGCAGAA CAAGCATCAT GTGCAAAGCT CGTGGTGAAC 420
CGGGGAAAGC ACAAAGCACC CCCGTGATGG AGGGTGGGGG TAGGGTAGGA AGAGAGGCTG 480
GCAGGGGGAG GGCGACTCTC TGCTTCCTCC GGGGGCCTCT GTGGCTCCGT CTGTGGCTGT 540
CCAGAGCAGT TGCCAAGTAT GCCCCTGGGG CCTGTCACTT CTTCATGCCT TGGTTTCCTC 600
ATCCATGTAA AGGGGGCAGT CGTGGCCCCT CCCCACCCAC CCGGTGGTCA AGATGCCTTG 660
GGGAACCTGG CATAGGGCCG GCCCTTCAAA TTTCTTTGCT CTGGTCCTCA CAGAGACCCC 720
AGGGCCACGT GATTTGTGGT GTGGTCCCGA AAAGGCACTG AGGGATGGTG TCGGGAGGGG 780
ACCCCATGTT GCTGCCTTCA AACCCTGTGC TCCTTCAGAT GAGCCCCCAG CTGCCATGGT 840
GGCATTCCCC GCTGGGCCAG 860
|
