| Tag | Content |
|---|
EnhancerAtlas ID | HS040-32893 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr8:22491070-22492450 |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr8:22492061-22492073 | CAAATCACTGCC | + | 6.04 | | ZNF263 | MA0528.1 | chr8:22491625-22491646 | GAAGCAGGAAGGAAAGGAAGC | + | 6.35 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65795 | chr8:22491770-22492448 | Pancreatic_islets |
|
| | 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 |
| GH08I022634 | chr8 | 22491771 | 22492448 |
|
Enhancer Sequence | GTTTCTGAAA GAAAGGTCAT CTTTTTTAGA ATAACTGGGG ATTTTCCACC TTGCTGGGGG 60
AGCGCAGGAG ATTCCACGCT CAGGAAAAGC ATCCCTCCAT TCCCCTCAAC TGTCCAGATC 120
AGTGGAGCTC ACAGTGTGGG CCTCAGCATC ACCTGGGAAC TCCAGGGACA CACATTTTCA 180
GGTCTCGCCC AGCTCATGAG TTAGTTGGAG GCTGGAGGTG GGGCCCAGCG GCCCACGGCA 240
CAGCAAGCCC GCCTACAACA CTGATGCCCC GTACATGAGA CTGATGTGGC TGTCAGGCTC 300
GCCTTGGCCC CATGACCACC ACCACCGCTC TTCAGAGGCA CTGTCTCTGC CCACATCCAT 360
TCCTGACTGA GGACAGTAGT GTTAGGCTTC TGCAGTTACC CATTCAACTC TGGTTTCTCT 420
GCTGGGAAAC TAAGCTTTCC ACAGCCATGG ACGGTGCGTC ACGGACCCCT GATGCCCTCC 480
TTGGTTCCGT AGCAAGCCAC TGTGAACACA GCACACCCTG GCTTCGTTTA TGCTCTGACA 540
ATGCAGCTGT CTGCAGAAGC AGGAAGGAAA GGAAGCAATG GCTCACAGCA GCTCCCGAAC 600
TGGAAAGGCA GTGGGGACCG ATCAAGAAAA ATGCGACCCA AGTAACTCAG ACCTGAAATA 660
ACTACAAAAC AAACAACTGC AGACAAACTC CCAAATCCAG TCCTTGGCTT GTGACACACA 720
TAGTTTGGCA ACGCTAGAGG CCAGGAGCAA GGTGCATGTT CAGACCAGCC CACGGCCCAG 780
GAATTAGCAC TGGCATGAAA ATTCATGGCA CAGACCAAGA CGGCCACAGT CCCTGCACAG 840
GCAGTCAGCG CTCACCCGGG CATGGTGGTG GTGACGGCGG CTCCCAGGGA AGGAACGCTT 900
TCCTTTTGTG ATCAGTGCTT TGTAGGAAAG GTGTGTTTAC ACATCAGTAA CTGGCTGAGG 960
CTTAGGAGCT GGCATAAAAT GGGAACAAAT TCAAATCACT GCCTCTATTG GGACATTTCA 1020
AGGGTTTTCC TCGTAACTGC AGTACCAAGT AGGAGCACAC TGGTCCTCAA GTCCCACCCG 1080
TAGGTGCCCA CTGCCCTGTG GCCCTTTGAA TGGTGTCAGG AGACAGTGAG GCCGCCCCAT 1140
TTGCACTAGG CTCACAGACA GCCAAGCAAA GAGTGGATGG GCAACGGTTC CGGAGTGGGG 1200
GCTGTTTCGG TCACCTTCTA GTTTGGTGGC GGGCACGGGG GTGGGCAAAG GAATGAGTGG 1260
GGCATGGGGA GGCTTCGCTG TGGAGACAAG GCCCTGGACT TGGAGAAGAG GAGCTGAACT 1320
CTTCCTCCTT TATCAAATGG ACATGCCCAT TTATAAAATG GGTGTGTCAT GTGCCCTGCC 1380
|
