| Tag | Content |
|---|
EnhancerAtlas ID | HS121-13656 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr16:4939060-4940180 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr16:4940126-4940141 | TGACCTCTGACCCTC | - | 7.34 | | Nr2f6 | MA0677.1 | chr16:4940126-4940140 | TGACCTCTGACCCT | - | 6.93 | | Rxra | MA0512.2 | chr16:4940126-4940140 | TGACCTCTGACCCT | - | 6.73 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65358 | chr16:4939432-4940498 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH16I004888 | chr16 | 4938742 | 4939110 | | GH16I004889 | chr16 | 4939433 | 4940498 |
|
Enhancer Sequence | TTCTGTAAGA CAGAGTTTAA AAATCAAAAC TAACCAGAAA AAAAATTTAA AAAAGCAACC 60
ATGGATGCAG TAGCTGGAAA TCTCAGAATC TGAATTTATT CTTCTCTAGC ACAAAGTATG 120
ATGAATGGCT CCCTTGTATA CATTTTTATT CATTGCAAAA GGCAGTTTTT TTGTTGTTGT 180
TGTTTTTTTT TTTTTTTTTT TTTTTTTTTT TTTTTGAGAC AGTCTCACTG CATCGCCCAG 240
GCTGGAGTAC AGTGGCGCGA TCTCAGCTCA CTGCAGCCTT AGCCTCCTGG GTTCAAGCAA 300
TTCTCCTGCC TCAGCCTCCC AAGTAGCTGG GACTACAGGC TCCTGCCACC ATACCCAGCT 360
AATTTTTTTT TGTATTTTTA GTAGAGATTT GGTTTCATTA TGTTGGCCAG GCTGGTCTTG 420
AACTCCTGAA CTTGTGATCC TCCTGCCTCA GCCTCCCAAA ATGCCGGGAT TACAGGTGTG 480
AGCCACCGCG CCCAGCCACA AAAGGCAGTT CTAAGGCTCT GTGAAGAAGG GCCAAGATCA 540
TTATCTCTGC TAGGAAACAA ATGTTTACTG ATGATTTGGA CCACCAGACA CTGTTCTGCT 600
GTCTGACTTA GATTATCTCA TTTAATCTTC AAACGATGCC AGGAGGTAAG CATCGTGACC 660
TCCAGCTTAT GAGTGAGGAA AGCTTCTGAG GTGGGGATGT GGCTGATGGG GTGGACCCGG 720
GATTTGCATC TCAGCCATTG GCTTCCCGTG TTCCTCCCTC ACCCCAAGGC ACTGCGTTGG 780
GCATGGGGGA GGCAGGAGTC CCAACTTTGA AAATGGGATT TCCCCCACAA AGGCGGCTCC 840
TCATTCTGTA GCTGTTCACT CACATAGCCA ACCCACGCCA AGTGTCCATT CTGCACCAGG 900
CCCTGTGCGG GGCACTGAGC TGGGAGAGGT GAGCGACACA CTCGGTTCTT GTTCTCAGAG 960
GGTTGGGTGT TGGGAGCTTG AGCTGAGGCC CAGGGAGGAC ACAGCTGTGG CAGGCCTCTG 1020
CCCTGCTCCA CCTCCCAAAG GCTTGGCTCC CCAGAAAGGG GCTTGTTGAC CTCTGACCCT 1080
CCCTTGCCAG TGTGTGCCTG GGGCTGCGGA AACGGCCATC 1120
|
