| Tag | Content |
|---|
EnhancerAtlas ID | HS184-16460 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:73418670-73419200 |
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 | chr2:73419073-73419094 | GGTGCAGGGGAAGCAGGAGGG | + | 6.25 | | ZNF263 | MA0528.1 | chr2:73419082-73419103 | GAAGCAGGAGGGGCAGGGGAG | + | 7.07 |
|
| | 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 |
| GH02I073191 | chr2 | 73418261 | 73419727 |
|
Enhancer Sequence | CACTGCACCT GGCCTATGAA GTTATTACTA ATCTCTCCAT CCTTTGTACT CCCATAGAAT 60
CCATCCCTTT GGTTTGGCAG TTGCATTAGC TAGTTGTGGA TGAGTCTCTC TGTCCCCTCC 120
CTCCACCCTC ACCGTAAGAC TCTGAGCTCC CATTGGGCAG GAATTGTATA TTTCATTGCA 180
CTTTGTACCC CTCATAAAAC CCAACACAGA ATAGGCCTCA AACAAGTAAA TGTTTGTCGA 240
CTTCAGTCTA ATTGAAGGGC ATAGAATTTC AGAGAAAATC TTAAAGGCAG CATACATAAG 300
AAAAAGTTAG GAAACACTAG GTAACTGCAA AGTGCAATGT GTTAGCTGTG CATTCCAGGG 360
AGGGAGGAAC AAACAACCAA CCTTGTTTGC TCTTGGCCTG TCAGGTGCAG GGGAAGCAGG 420
AGGGGCAGGG GAGGGGAGAG CAGGTGTGGG CTGGAGCTGA GACAGCCCAG GCAGGGGGTA 480
GGGGGAGGTG GTATGGGGCC TCCCCAAGGC AGCTCTGGGG CCCTCTGACC 530
|
