| Tag | Content |
|---|
EnhancerAtlas ID | HS040-15740 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr17:54776190-54777350 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr17:54776336-54776347 | GTCAAGGTCAT | + | 6.32 | | Esrrg | MA0643.1 | chr17:54776337-54776347 | TCAAGGTCAT | + | 6.02 | | RARA(var.2) | MA0730.1 | chr17:54776329-54776346 | AGGCCAAGTCAAGGTCA | + | 6.36 |
|
| | 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 |
| GH17I056697 | chr17 | 54774751 | 54777998 |
|
Enhancer Sequence | ATTCACACAG CTAGTTGGTA AGGGGGGCCT GGATCCAAAT TCTGTGCTCC TTTGATTTCA 60
CTATGCTCTA TTTCCACCGA GGAAGTGGGT TCCCTGGTGG GGCCAGGGAG GTGGCTCTAT 120
GGCTATGAGC CAAGATTTTA GGCCAAGTCA AGGTCATGGA CTCTTGGGAT CAGCCCTGGG 180
GCCAACAGGC TGCCAGAAGT GACAGAACGA AGAAAGGAAA GGAAGGAGAG AAACAGGAGA 240
CAAATCTTGA TGGCTTCCCC ATATTGCCAT TGTCCTACTT GGGGAGTTCC ACCTTCATCT 300
GTTTTACCCT TTTTTTCCTT TACCTTCGAG CTCTACGTCT CTTTATCAGT AAACTAGCCT 360
TGCAGACAAG TGCAAACTGT GCCAGCCCTT AGGCTGCAAA GGAAATGAAG TTGGCATTCT 420
GTAGTCCTCA CCTGGCATGA ATCACACACA GCCCCAAGGG ACCGGGACAA GGCTACATGT 480
CAGACTGATG GACTATTGTC TGGAGCTTTG AGAGAGGAAA AAGGGAAGGC TGCTTGCAGG 540
AGAAAGGTGA ACAGGTTGGC CCCGGCCCAA GAATGACAGA GGCGCCTTGC TCCTGCCACC 600
CGGCTCTGCT CCTCTGGCCC AGGAACAATA ACAAGGCGCT GTCAGGAAGT GACACTAAAA 660
TGCCTTTCCC CTTATACCTC GTTCAGCCTC TGGCAAAAGG AGGTTCCCGG AGGGAATATT 720
TTTAGTTTGA CAAATGAAAG CCTGGGACCG AGGACAGGAG GGATAAAGGG AGCTCTTCTC 780
TGACACTCCT GGAGACGGGG AGATGATGAG TCAGATACAG AGGGCTTAGG CACGACTTCT 840
CAAGACATTC CTCAGGCATG AGCACAAGCC AGCCGCTCGA ATTCCTCCTG CAAGGCCCGC 900
CACCCGGCAA TCAGGGCGGA GGGGCCGGGC CAGAGGAGCA GCTCTGCTCT GTCTTCCTCT 960
TGGCACATTG TTGGACAGCA GCTTTGGAAG ATCAAAGCAG CCGCCTGTGT TGCTTTCCGG 1020
AACTGGGACT CAGGAGGCCT GGGTTCAAGT CCAGGCTTCA CCATTTGCCG GCTGTGACAT 1080
TAAGTGTCCT CATTTCTCCC TTTATGCCTC AGTTTCCTCA TCACCAAATT GAGAGTATTA 1140
TAACACCTTG GAATTATTAT 1160
|
