| Tag | Content |
|---|
EnhancerAtlas ID | HS040-00019 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:1174760-1175470 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:1175345-1175360 | AGGGGTCAGGGGTCG | + | 6.54 | | NR2C2 | MA0504.1 | chr1:1175331-1175346 | TGGGGTCAAGGGTCA | + | 6.61 | | NR2C2 | MA0504.1 | chr1:1175338-1175353 | AAGGGTCAGGGGTCA | + | 6.65 | | Nr2f6 | MA0677.1 | chr1:1175332-1175346 | GGGGTCAAGGGTCA | + | 6.81 | | RREB1 | MA0073.1 | chr1:1175145-1175165 | GCTGGAGGGTTGGTGGGGGG | - | 6.08 | | Rxra | MA0512.2 | chr1:1175332-1175346 | GGGGTCAAGGGTCA | + | 7.1 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_41703 | chr1:1174282-1177679 | LNCaP |
|
| | 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 |
| GH01I001235 | chr1 | 1170967 | 1178914 |
|
Enhancer Sequence | CGCCCCCAGG GGCCAGGCCA GGGCAGCCGC ATCTCCTACG TACCCCAACA GTGGGGCCCT 60
TGAGGCACCG GGGACGGATG GGCAATGGTG TCCACACCTG ACAGGCGGGG CCGGAGCGGG 120
GCCCAGCCTC CTCCTCACAG CCAGGAGCCC CCAGCCCTGC CTCCCCTGGC TCCTGCTGCC 180
CCCTCAGGGT GGCTGCCGCA CCTGGCCCCA AGAGGACTTC CTGGCTGCCC TGAGCTCCCG 240
TCCGCATTTC TGTCCATTCA AGACCAGGAC AGCACCAGGG CTGGGAATAC TGGCTCCGAC 300
CCAGCCGAGG CAGCCCCGGG GCAGGGTGGG TCAGGCAGGT CCAGCGCTGG GACTCTAGGG 360
AAGGGCTGGT CCTGTGAGCA GACGAGCTGG AGGGTTGGTG GGGGGAGTGT CCCCGCACCG 420
GGCATGGCCC CTCCCAGGAT GGCAGGGAGC CCACGGCAGG AGTGTCCGAT GCCCCCAGCC 480
CCGGCCAGGC AGCAGGGTCG GCCTGCGGTT CTGGGAAGTC AGCCCTGGTG GAGGTCACGG 540
AGAAGCCGGC AGCTCCCTGC CGCTCAGGGC ATGGGGTCAA GGGTCAGGGG TCAGGGGTCG 600
GGTTGAGGCC GTCCGGCACG TAGCCGGCTG CTCTGGCTTT GCTCCTGCCA GGGTCCACGA 660
AGCTGCCAGA CGCTTGGGAC ACTCAATACC CCAGCTCCCA AACCGGGGGG 710
|
