| Tag | Content |
|---|
EnhancerAtlas ID | HS040-00477 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:12112020-12112710 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFF | MA0495.3 | chr1:12112307-12112322 | GTGCTGAGTAAGCAG | - | 6.33 | | MAFF | MA0495.3 | chr1:12112307-12112322 | GTGCTGAGTAAGCAG | + | 6.48 | | RARA(var.2) | MA0730.1 | chr1:12112124-12112141 | TGAGCTCTGCCTGACCT | - | 6.22 | | ZNF263 | MA0528.1 | chr1:12112469-12112490 | CCTTTCTCCCCAGCCTGCTCC | - | 6.2 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_32538 | chr1:12111224-12119174 | GM12878 |
|
| | 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 |
| GH01I012051 | chr1 | 12111817 | 12113781 |
|
Enhancer Sequence | CCTGAGTTCT GAGGAAGGCG ATGGGACCAG CTGCCACAAG GCGAAGCTGC CTTGCCACCT 60
GGGGCCTTGC AGGGTTGAGC CCCGAGCACA GGGGCCCTGG TAGTTGAGCT CTGCCTGACC 120
TGGTCATTCT GAAATCAGGG GCCCCTCCCA GGAAGGCTGC GGGCCCAGGA GAGCAGCGAG 180
GCAGGCTCAG AATTGGGGCT TGAGATGACT CATCTGTGGC TATTTATTAC CCGTCTCCAT 240
TTCTCGGTCT GATTGGGCTG CTCATGGCCA AGCCTCCCTC CCTGTTGGTG CTGAGTAAGC 300
AGCCTGGACC CGTCCTGCCC CTCTGGCCTC ATCTGGAGCT CTCTCCTTTC CCTGTCAGTA 360
ACCCTCGGGC CCCCCTGGGG CCACTGAAAG TTCCCCCAGC CACCCTCAGC GAGCTCTTCC 420
CAGCAGTCCC ACTCTTTGCT GTTCTCACCC CTTTCTCCCC AGCCTGCTCC TTCTTTCAGG 480
TCTCAGCTTG AGCCTCACCT CTGCCAGGAA GCCCTCACTG ACCACTGCAT CCACCCCACC 540
ACAGTCTGGG TAGGTGGCCG CTGACAGGTG CTCCTAAAGC CCCTGCCCTC CCTCAGTAGT 600
CCCTCCTCAC CCCAGCTGAA GGCAACGTCA CTCTTCCAGT TTCCCAGGCC AAACCTTTGC 660
CTCATTCTCG CACACATCCA ATCCTTCAGT 690
|
