| Tag | Content |
|---|
EnhancerAtlas ID | HS184-11886 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr15:101233530-101234260 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr15:101233825-101233846 | GGAGCAGAGAGGAAAGGAGGG | + | 6.81 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_45862 | chr15:101234108-101237664 | Osteoblasts | | SE_55705 | chr15:101226004-101233621 | u87 | | SE_55705 | chr15:101233873-101235223 | u87 | | SE_67543 | chr15:101226004-101233621 | u87 | | SE_67543 | chr15:101233873-101235223 | u87 |
|
| | 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 |
| GH15I100693 | chr15 | 101233795 | 101233950 |
|
Enhancer Sequence | CCTCATAGAA TATTCCTCAT AGAAAAAAGG TAGGTGCTAT TATCATCTCT ACTTTAGAGA 60
CAAGGAAAGT AGACTTAGCA AGAGGAAGTG GCTCTCCTCA GGCCACATGG GTAAAGTGGC 120
AGAATGAGGC TCAAACCTGG GGCTGTGCGG CTCCACTGTC CACATACCTC CCACGAGCTG 180
GTCAGCCTCT GAGTGATAAT AGTGGCTTTG AAGGCTTAGA GGGAATGGCT GTAGCTGGGT 240
GTCCAAGCAA GCCATATCTG TAAAATGAGT GCCTTCTAAG TGGGTAGAAC TCAGAGGAGC 300
AGAGAGGAAA GGAGGGAAAT TCCAGGTGGG TTGGGCCAGG AGTGCAAACA TACATAACTG 360
GTTTGATGGA TGGAGAGTGA ACAAGTTTGG CCAGAATCAA GCAGCGTTTC TCAACAGGGG 420
CACCACTGGC ATCGGGATGA GACAATTGTT CAGTGTGTGG GACTGTTCCA GGCATTAGAG 480
GGTAATTCTC ATGCCTGGAC CCTGCCCAGT AAGTGCCACC CCCATCCTAA TGACAATGAA 540
AATGCTTCTA CCCATTTCCA AACACCCTCT AGGGCACCCC AGGTTGAGAA CCACTAGAGA 600
AATGAGAGCT GGAAATCAGC TGGGGACTGT TATTGGGATA AGACTGAGGA GGGCCTTGAA 660
AGCCAAACAA GGTTAGCCTT GAGACTGGAG ACGATGGGGA GTGACTGAAG GTTTATGAAT 720
GAAGAAGAGT 730
|
