| Tag | Content |
|---|
EnhancerAtlas ID | HS121-18889 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr19:4365620-4366490 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26598 | chr19:4364974-4366059 | Esophagus | | SE_26598 | chr19:4366396-4381720 | Esophagus |
|
| | 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 |
| GH19I004364 | chr19 | 4364975 | 4366059 |
|
Enhancer Sequence | GGCTGGGATA GGATGGCCAG GTGGGTGTGG GCTGTGAGGC CTGCACTCCT CTGCCCTGGC 60
AGACTGCAGC CCCCACATCT CCTCCCCACC CTTGCTTCCT GTGCCTGTGG ACAGCCTAGG 120
CCACACAAAG CACAGTGGAA TCCCCAGAGG GTCCCTTCCC TGCTCCTGCT AGCCTCAAAG 180
GAGCTGGCAG CGGGTGGAGA GGTGACCAAG CTCCTCAGGG GGCAAAACCT CCTCCTTCCA 240
AGGGCTGCTC CTCTTGGAAC GTGGCTATGA CCCCTCATCT GGGGGGTGCC AGGGAGGAGG 300
CGCAGCAGTG ATGTGCAGCG GGGGGTGGTT GAGGCCAAGG CTCCCGGGGT GGGTGATGAG 360
CTGTGTCCCT TCCGCTGCCC GCTTGGGTCT GCTCCTGGCA GGGCCTGAGT GGACACTGCT 420
GGGTGTGCGT CTGCCCCCTG TCCGTGGCCT CCTATGGAGC CAGCATTTGG GTTTTCCTTG 480
GGGAAAAGCC CGTCTCTCAG CCAGGGAGAC CCAGTCCCAA GCCCAAGAGG TGAAGTCCAG 540
GCCAGGGGCA CTGGGGAGGG GCGGCCAATA CAAATGGATC CCACAAGTAA GCTGGGGGAG 600
AGGCTCCCTG CCAGGACTGC TGGCTGGAAG AGGGGTTGAA GGCTGGGACG GCCCTGAGGA 660
ACCAGTCGGC ATGAGAGTGA AGCCAACAGA GGGGCTGAGC TGCTGGTTGA GGTGGAAAGG 720
CAGCATGCAG CACCAAGGAT GGCCTCTGCA CTCCGGGATC CAGCTGTGCC TGAAGCCCAC 780
AACCCATGAG CCTGGCGGTT CTGTCATCCC CTGCCTTCCC TCTGACACAG AGGCCAGAGG 840
GCCTGGGGCA GGCCCTGGCA GTGGCTGGAG 870
|
