| Tag | Content |
|---|
EnhancerAtlas ID | HS121-25388 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr22:24944040-24944880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr22:24944092-24944103 | CTGAGTCACCC | - | 6.02 | | JUNB | MA0490.1 | chr22:24944092-24944103 | CTGAGTCACCC | - | 6.02 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_23474 | chr22:24944365-24948308 | Colon_Crypt_1 | | SE_31995 | chr22:24944357-24948395 | Gastric | | SE_41463 | chr22:24944741-24948264 | Left_Ventricle | | SE_50904 | chr22:24944466-24948467 | Sigmoid_Colon | | SE_52895 | chr22:24944429-24952524 | Small_Intestine |
|
| | 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 |
| GH22I024547 | chr22 | 24943405 | 24944069 |
|
Enhancer Sequence | CCTGCAGGTA GACGAGCTGG GGAGCTCAGC TTGGTCTTGA GGGTCAACTG GTCTGAGTCA 60
CCCTCCACCC ACTGGCCCAA GAGCCCCGTC ACAGGTCCCA TTCCCCAGAA GTCTCCCTCC 120
TTCATCATGA GACCCTAGGT CCTGCCCACA CACTGCCCAG GCTGCTTGGG GCACCGTCCT 180
GGCTCCAGAG TTGCAGGCCT GGACTCTGCT TCTCAAATCT ATTGTGTCTT GTGGGCTGTG 240
ACCTTGAGCA AGTCATTGTC TTCTCTGGCC TCTTTAGCTT CATCTCTAAA ATAAGGTCCC 300
TGATCACATC AGTGGTTTTC AAAGTTTTAG GCAAAGAACG CTTTTGTTGA ATTTTCTCTT 360
GCTGAGATTC CCAGGATGTA AAACAGATGA AGATGCAGCT GCCCTGTGGT TCCAGGAAGC 420
CAAATGAAAA ACTCTTGTAC AAGGTGACGG CTACAGTCCC TCTTGGCTCT CACTGTCCAG 480
GTTTCTGTGA TATTCACACA GCCTCAGCTT AACGGTCAGC ACCCCATTCT CCCAGGAGCC 540
AGAAACTGGG GAGTGGAGGG CCTCCTATCC CAGTCACAGA ACTGCCTTGT AGGACAGGCC 600
TGGGCACCTG GGACTTCCTG GCCACCCCAA GCCCCCAGAC ATTACTATCA TGGAGAGCTG 660
GAAGGCCTGG TCCACCCCTT GCTCACTTTT GCAGATGGGA CTAGGACCAG GTAGAAGCTT 720
GGCCTCCTGC AAGCCCCAAC CAAAGATAGC TACATGGACC ATGGATCCCA CCCAGGTCTC 780
TCCCAAGCCA GAGCAGAAGA TGTAGATGGG AAGCACCTGG GCCCCCAGCC CTGGCCCCAC 840
|
