| Tag | Content |
|---|
EnhancerAtlas ID | HS184-32444 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chrX:152933000-152933870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chrX:152933395-152933406 | GCAGGGTGTGG | - | 6.62 | | MYC | MA0147.3 | chrX:152933584-152933596 | GGCCACGTGCCT | + | 6.07 | | REST | MA0138.2 | chrX:152933439-152933460 | GAGGCTGCCCAGGGTGCTGAA | - | 6.81 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chrX | 152933025 | 152933200 | | chrX | 152933200 | 152933396 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH0XI153667 | chrX | 152933056 | 152933744 |
|
Enhancer Sequence | ATGCTCTCTG GCTACAAACC CCTTCGATGG CTCCCCACTG CTCCTAGACT ACAGCTCCAG 60
CTCCTTCCCC TGCCAGGCTT GGTCTGGCCC GTTCCTCTTG CTGCCAGCCT CAGCACCAGC 120
CCTGAGCCTG AGAAGCCCTC ACAGTGTCCA GCACAGCTCC CTTGCCATCA CTTCACACAC 180
ACACACCACC TTTTGCCTTT GGCTAAACCA GTCCTTTCTC TCTCCCAGGC TGCCATCCCA 240
CTGCCTAGGT GACCCAAACT GCCTTCCTCA TATGCGGTCT CGGAGGGATG AAGGAGGGGT 300
GCCGCCTCTG CTTGACCTGG GGGTTCCCCC TCTCGCCCCT ATCACAGATG GGCAGGACCT 360
CTCCCCCAAG GTTGGACTTC CCCAAGGCAG GATTTGCAGG GTGTGGGGTA GGGGCAGTCG 420
CGGAGAGGAA TGGATTTGAG AGGCTGCCCA GGGTGCTGAA GGAACTAGGG AGGCTAATGG 480
ACGTCTAAAG ATGGGGCCGT GGCTCCCCCT GCTGACGGGA GGCCATATTG CACCCTGTGT 540
CAAGGCAGCC CAGAGCTGGC TTAAGCTCCA AGCCGAAGCG ATCTGGCCAC GTGCCTGGAC 600
TGGAAGAGCT GGCTGTTCTG AGCGAGTGCC GGTTTCTTCT GTAAGGCTGG CTCTGGCACT 660
CCTGCTCATT GCTCCCAGAC CCACAAAGAT CATTTTTATC ATCCCCGTAA AACCACCCCT 720
CCAATAGAGG GCGTCCTCCT GGAGGGCAGG CGCCTCTTCT GATAGGCCCA GGTCAGTGCC 780
CAGCACCTGG CCCAGAGTAG AGGCTCAGTC AACATCTGAC CAAAACAACA GCAAGTAGGT 840
ATCGTGGGAG TCCAGTGTGA ACAACAGAGA 870
|
