| Tag | Content |
|---|
EnhancerAtlas ID | HS040-23671 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr22:19675580-19676700 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr22:19675781-19675799 | GCTTCCTTCCTTCCTCCT | - | 6.96 | | EWSR1-FLI1 | MA0149.1 | chr22:19675777-19675795 | CCTGGCTTCCTTCCTTCC | - | 8.7 | | RREB1 | MA0073.1 | chr22:19675587-19675607 | GCGTGGTGGGTGGGGCGGGG | - | 6.17 | | ZNF263 | MA0528.1 | chr22:19676137-19676158 | TCCCCCTCAGCCTCCTCTTCC | - | 6.07 | | ZNF263 | MA0528.1 | chr22:19676134-19676155 | GCCTCCCCCTCAGCCTCCTCT | - | 6.11 | | ZNF263 | MA0528.1 | chr22:19676140-19676161 | CCCTCAGCCTCCTCTTCCCCC | - | 6.33 |
|
| | 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 |
| GH22I019687 | chr22 | 19674724 | 19676523 |
|
Enhancer Sequence | GTCAGAGGCG TGGTGGGTGG GGCGGGGAGG GGTGTCACAG CTGCAGGGCA GCCTTGATGT 60
CTGCACTTGG CTTTTTAATT TGTAGTCACA GCCAACAAGT GTGGAAACCG CCTCAGGACC 120
GGCTTGAGTG GAGCGGCTGC GGGAGTTACT TCATGACTGT GGTCTCACGC TGTGTTTCGC 180
CACCCATCCC TGCCTGGCCT GGCTTCCTTC CTTCCTCCTG GGTACGTTGG CCCTTGGCTC 240
TCTCCTCATT AACTGGCCCC TCGGACCCCG GCTGGCCAGC TGTCTGCAGC CTCCTGGGTG 300
ACACCTTCAC CCCTGCCTCC TCGGGGGTCT GCTGCCGCCA CATCAATCTC CCTAACACCC 360
TGGGCATGCC ACCCCTCTGG AGACCTCCCT AGTCTCTCTC GCAGGGCCCC CAACCTGCTC 420
AGCCCAGGCC CACTGCCCTC TCCCTGCCCG GACACGTGCT CCCGTGGCCC GGCCGTGCCT 480
GCCCACACAC CTGCCCTCTC TGAGGTTCAC ATGTGGCATC CAGGGGCCCT TCCCCAACAG 540
CTCTGCCTGG TGCAGCCTCC CCCTCAGCCT CCTCTTCCCC CCGAGCAGGG TTTGCAGAGG 600
CCCAGAGGCT GCCGGGATGA GTAGATGTTG GGATCCTGCT TACTGGGCGT GTCTTATCCC 660
CCAGAGCAAT GGCCTTGGAG GTCAGGGACC CAGCATGGCC ATGCTGGCTT GGGGTTTAGG 720
AGCTGTCTCA CCAGAGCCCC GCCTCAGCCC ACAGCCCCGG GCCTGTTTCC TTGAAGGCTC 780
CCCAGAGCCC CATGCCTGGT TTTCTGGCCA GAGCCCTTGG CAGTGACCCC TGCTCTCCGC 840
CTGCAGCTCT GGGCGTCCTC TCAGCCCCAA GCCCTGATAG GTGCCCCCTG TCTCTGTGCC 900
TGCAGCCTTC AGGAGTGGCC CACACATTGG CTTTTATCTC TGGGCTCTCT GTCACCTCCT 960
CTCCCTCCTG CCACCCTCTG CTCACAGGCT GCGGGTGTGG GGCATCCAGG AGCTGGCCGG 1020
TGGAAAGAGG AGCAGGTGCC CTTACGCAGT GGGGAGCAGA CACACTTGTG CTGCTTTTCC 1080
CTTGGGGCTT GGGGTGGCCA CTGGGGCAGG ACATGAGGAC 1120
|
