| Tag | Content |
|---|
EnhancerAtlas ID | HS040-34029 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr8:143764650-143765630 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr8:143764741-143764752 | GCTTCCCGCCC | - | 6.02 | | Sox6 | MA0515.1 | chr8:143765274-143765284 | CCATTGTTTT | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_31467 | chr8:143755671-143766550 | Gastric | | SE_34702 | chr8:143755775-143766731 | HeLa |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 143764831 | 143764997 | | chr8 | 143765021 | 143765630 |
|
Enhancer Sequence | TGTGCCCCGT GAGCATCCCC AGGCCCCTGA GTGGGAGGAC ACCATCCACA CTTGCCTTCT 60
GCGCTCAGGG GAAGCCTTTT GCACACAGCC TGCTTCCCGC CCTAGGGCTA GGGGTGCAGC 120
CTGTGACCTG GGTGGGGACC TGCTCAGGGT GAGGCCTCCA AGGGTGTTAG GGGTGGGGCT 180
CGGGGGGCGG TTTCAGAGAA GAGGAGACAG AGGCTCAGGA AAGGGAACGG GTCTGTTGCC 240
CACATCCCAT ACCGAGCCAG GATTGGAACC CTGGCCTGGA GCTCTGAGGG TGGGTCATGG 300
AGCAGACAGT GGGCAGAGCT GTGCTGGAAA GAGCCAGGCC TCCCGTCTGA CATGTGACTT 360
CACGGGGAGA CCTCCCTCCT GAACACTGGG GGCCCAGGGT GGCATTGTCA GCAGGGTGCA 420
GCTCCCCAGG CCAGCATCTG AGTGACCCTG GGCACTGGTC ACACCCTCCC CGCCTCGCCT 480
ACACCCAGCC CAGCCTGCCC GGCTTCCATG GTGAGCTCTG GGCTTCCATG GTGAGCTCTG 540
CCCAACACCT ACCCACCCTC CCAGGCCCAA GGCACACTCA GACCTGCCTT GGCCCAGGGC 600
CTGAGTCCAG AGTTGAGGGC TAGGCCATTG TTTTCTGGGA GGGCCCTGCA GACCTGGGAG 660
CCCGCACAGA ACTCTCCACC CCTCAGGGCT CAGGTGCAGG AACTGGGGCC TGAGGCTCAG 720
GCAGGTGCTT CTGGCCACAC TGTGTCTCCT GAAGCTGCCG GCCCGGGCTT GCTGACCTGC 780
TCTGGGGAGC ATCAAGGACG CTGAGTGAGG GAGGCTGGTG CCCTGCCTGG CTCCATCCAC 840
TTAGCACACA GTTATCTAAC CCTTGGTATG GTATGTTCCA CTGCTGTTTC AGTTGCTCCT 900
GGTCACCCTG GTGATAAAAA CTGGGAGAAA AAAAGGAAAG CAAGGAAAAA GGATCCAGAA 960
TGCTGAGATG GCCAGGGAGG 980
|
