| Tag | Content |
|---|
EnhancerAtlas ID | HS040-26078 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr3:125847960-125849060 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr3:125848270-125848285 | AGGTCACCCTGGCCA | + | 6.25 | | ZNF263 | MA0528.1 | chr3:125848717-125848738 | TCCTCTGCCTGTTCCTCCTTT | - | 6.04 |
|
| | 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 |
| GH03I126129 | chr3 | 125848461 | 125848610 |
|
Enhancer Sequence | GTCCTCTGTG GGGACCCTGG AGGCGATGCC TCCACCTGCA GCCTGGCTCC TCTCTGGGGC 60
TCTAAGGGTC CACAGCCCAC TTTCCCACAG GAGCCTCCTC CAGCCCGTGC TTGAGGAGTT 120
GGTTGTTCAT CTGCATGAGC TGTCAGTGAC ACAGGGACAT TGGAGCACGT TCTCCTTGCA 180
AATACTCCAA CATTCAGGTG GAGCTGAGGG GCCTTTGGCC ATGCCCACAG CTGTGAGGTC 240
CCCTACCCTG CAAGGGGCAC AGAGCAGGTG GGAATGACTG TGGTGCTCAT GCCAGCTGGG 300
CCCTGCTCCC AGGTCACCCT GGCCAGGCTC TCCTGTGGCA CCGCGTGCAG GCGCAGTGAG 360
GGTGGACCCA GGGCTGGGGC TCTCTAGGTC CAGTTGCAGG CGCATCCTCA GTGCAGATCA 420
TGGATCAGGG CTGCACCAGC ACCTGCTGCT CTGGTGTTTG CTGTCACCGG CCTAGCACAG 480
TGGCCATGCA CTCTTGGGTA AGCCTCCTCA GGCACGCGTG TGAGTAACTC ACCAGGACTG 540
GGGCCAAATC AGGATGTATG GCCTCGAGAG GTCACTGCCC AGTTTCCTCT AGCAGGGAAA 600
ACCCAGAGCC CGGTGGCTGT GTTCCAAGCC CTTCTCCCTA CTCCTGCCCT GGGGCCACTG 660
GGTGGCGAGG TGAGGTGCCT CACGCCAGGT TCATTTCCCG GCGCCTACAT GCTTGGCATC 720
CAGCGGGGTC CGAACTCCTC CTGCTGAGCA GCTCTCGTCC TCTGCCTGTT CCTCCTTTGT 780
TCTATATTTC CTGTTCCTCA GTGCTGTGCA GGAGTTCCTC ATCTTTATGA ACACTGACCA 840
CCATACCCAT TTTGGACATT TTTTGGGTTT ACTCTTGTTT CCCACCGTGG ACCTGACTGA 900
TCCAGTGTTA CTGGGAGATT AAATACAATT GTCCTCAAGT CCTTACAACA ATGCCTGGCA 960
TGGAGCAGGT GCTCAAGAAG CACATGGATG GCTGTTTGAT AAATGCACGC ACAGGGTGCT 1020
GTGAGCTCCC GCAGGCTGTG CTACAGTTCC GTGTACTGCA TGGAAAGCAC CGCGAGGCTG 1080
CACCTCGCCC TGGGCAGGAA 1100
|
