| Tag | Content |
|---|
EnhancerAtlas ID | HS050-05701 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:209584660-209585830 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:209585810-209585828 | CCTTCCTTTCTTCATTTC | - | 6.64 | | EWSR1-FLI1 | MA0149.1 | chr1:209585802-209585820 | TCTTCTTTCCTTCCTTTC | - | 7.14 | | EWSR1-FLI1 | MA0149.1 | chr1:209585806-209585824 | CTTTCCTTCCTTTCTTCA | - | 7.37 | | TP63 | MA0525.2 | chr1:209585168-209585186 | AACATGTTATGTCATGCC | + | 6.62 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_26692 | chr1:209584435-209592402 | Esophagus | | SE_33755 | chr1:209574939-209586916 | HCC1954 | | SE_35814 | chr1:209581893-209587003 | HMEC | | SE_64219 | chr1:209583527-209591639 | NHEK |
|
| | 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 |
| GH01I209409 | chr1 | 209582487 | 209591632 |
|
Enhancer Sequence | CCTTCTCTCA GAGCAAATAA TTTAGTCCAT CAACATTGTG CTTTCCAAGG AGGCTTATTT 60
TTTATCCTTC CTCTTTGCAA TATCTCCCTG TCCCCACTCT AGTAGCACAC ACACCAGCCC 120
CTTCCATCAC CCCTACAACT GCCACTGGCA CCACCGACAC TACCACCACC CAAGGAGAGC 180
CAGAATGACG ACCAGCTTGC TTCCCCTCAG CAGAAATGGG CATGACTACT CAAATGCAAT 240
ACAGGGTTCT TTACAGACAA CATGCTCAGA AAATGTTTTC TTAGCAGAGC GGAAGGCCAC 300
CCCCTACTTC CCACCAAAAA TATCTGGCCT CTCTCAAGGC TTTCTGAGCA AGTCCAGACA 360
GACAGAAAAG GGTTGTGAAA CTGAAGATGC CTCTTTATTT TTTTTTCTTG GTAGGAGAGT 420
GAGAAATGGG GAAGGAATAA TTTTACAACA ATGAGTTCTG TCAGGCTTCT TTTCCCTTTC 480
CAACAGTTCT AGGATCTAGC ATCAGCAAAA CATGTTATGT CATGCCCTGG TGAGGAGACA 540
AAAAGGGAAG GAATTCAAAC TGCAATGGGT GGGGCTTTAA GATGCGTGGC CTCTCTTATT 600
GCTATTTATT TCCTTTCTCA CTGGCCTTTG GAAAAAAAGA AAAAAAAAAC GGCAAAGGAT 660
TTGGGGGCTA CACCAAAAGA AAGTGAAGGA GCAGAGTATG TGAGAAACTG AAATCTATGT 720
AACTACTTGA AGCAATTGGA AGTTCAGCCC AAACCTCAAA TTCATTTTTG TTTTTCTGCT 780
AATTATCTGG CATAGAAAGC CAGCCCTGGG GCAGCTGCTT CCCAGCAAAT GGATCCAGGT 840
CTTCAGTCTG GATTGGGACC AGGCTTTGGA CAAAGGCTGT GTAATTTTCA TAGCTTCTTT 900
TGCCATTTAC AGAAGAAATG GGACTAGCTA CTCTTCCTTC AGGACAGAGC CAACAAATAC 960
AGGTTCCTAC TGTAGCTGCT GGGATCCAGG TTAGATAATG AAGTTACTGG CAGTGCATCC 1020
TGCAACAAAA GGATGTTGTG AAACATCTCC TCCAGAAGTC TGAATATCTG AAGAGTTTCT 1080
CATCTCTCTC CTCTGTCTTT TCTGACCCTT TCAGGAGGCA ATAGAGTTGC TAACAGCTTC 1140
ATTCTTCTTT CCTTCCTTTC TTCATTTCTT 1170
|
