| Tag | Content |
|---|
EnhancerAtlas ID | HS040-07119 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr11:76476760-76478030 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr11:76477509-76477526 | AAGGTCACACTGACCAT | + | 6.19 | | ESR2 | MA0258.2 | chr11:76477510-76477525 | AGGTCACACTGACCA | + | 6.53 | | Nr5a2 | MA0505.1 | chr11:76477503-76477518 | AAGGTCAAGGTCACA | + | 6.37 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26826 | chr11:76477083-76483151 | Esophagus | | SE_52588 | chr11:76477874-76485218 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 76477687 | 76477727 | | chr11 | 76477783 | 76477896 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I076766 | chr11 | 76477121 | 76477270 | | GH11I076767 | chr11 | 76477731 | 76477895 |
|
Enhancer Sequence | CTTAGGATGC ATTTGTGCTG GAAGAAGTCT TGGGGGATGG CAAGGGAGAA GAAATGGCAA 60
GTGTGAAGCC TGGAAGCATG GAAGTACCCA GTATGTCGGA GAAGGCTGAG CAGCGTCTCA 120
TACTGTTCAA CGCAACGGTT GTCGCCATCC TTTCCCCACT CATTCCCATC TTCACCATCA 180
TCATTGTTGT CATCAAGGCC ACACTTTCTG AGTGCTGACT ACATACCAGG CTCTGCGCCA 240
AGTGTTTTAG ACACACTTCC CTTTAATCCT TATTTTATCC TCACTATTAA TAACCTTCAA 300
AAGTAGGTAC TATTATTATC ACTGTTTTAC AGATACAGAA ACCGAAGTTC AAGCAGGTTA 360
AGAGCTCTGC TCAAGGTCAC ACAGCTGGTT AATGATCTGT GTGACCCAAG GACACTCTCT 420
GTTCACCACT CCAGCAGGGA GCTGGGCCAC ACTGATCTCA TCCCTTTCCA AGCCTCCCAC 480
CCCATCACTG TCTGCCTGTC TAAGGAAACT CCTTTCCTAA ATGAAAGGAC ATGCCACTGC 540
GAAGATGTGG GGTGGGCCCA GCCAGGGCAG CCAAGAGACC TGGGAGGGGT GAGGGAGAAC 600
ATTCTGACCA CATTCGCCCT TCTAGATCCG ACCAACACAG GGTTTGATTC AGCTCCAGCC 660
ACTGCATGTT GCTGGGAGAT CTTGTCCCCT CTTCACGTCT GCAAATAGGG AATCTGAAGT 720
CCCAAAAGGG AAGGGCCCCA TCCAAGGTCA AGGTCACACT GACCATCAGG GGGTCAACTG 780
AAACTACAGC TTAGACTCTG GGCTCCCAGA CCAGGGCCTC GCCCACTGCC AGCCTAACTG 840
CAGCCAAGGC TAATTTTAAG GGATAATTTG AGGGTGCTGG GAAGAGTTCC TCCTCCCCAC 900
ACAAGGGTGT ACCTCCCCAG GCTGCTGGTG ATACCTGGAA TCCCTCCAGA GGGCACAGGT 960
CATGAGCCCT GGGTTCAGGC CCACCGTCTC CTCTCCATCC TCCCTGGGAC CCTCCTGCCC 1020
GGGCTTCCTC GCCTTAGGAA ATGCACAAGC AGCCAGGGGC TGGCTCTGAG GAGGCTGTGG 1080
AAGGAGGCTG CCCCCAAACC TGGGCACGCC AGGAACAGAG AGACAAACAA GAGGCAGCAG 1140
AGCCCAGTGA GAGGCTAGTA GCCACATTGG TTTTAATCAG GCTCCACGCA TACCAACTGT 1200
GTGACCTTTG GGAAGATATC TAATTGCTGT GGGCCTCAGT TTTCTCAGCT ATAACATGGG 1260
GATGAGAGTT 1270
|
