| Tag | Content |
|---|
EnhancerAtlas ID | HS184-22396 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr3:197121410-197122380 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr3:197121579-197121590 | GATGAGTCACC | - | 6.32 | | JUND | MA0491.1 | chr3:197121579-197121590 | GATGAGTCACC | - | 6.62 |
|
| | 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 |
| GH03I197392 | chr3 | 197119359 | 197123101 |
|
Enhancer Sequence | GGATGGCACG GGAGCTGATT GTCTTGACGT TAAGTTCCTC GGTGAGGAGA GAACAGAAGT 60
TAATGGCACC CACCGGGCCT GGGTGGAGCC TCAGCACCAC CAAAGAAAGC AGATTCTGCA 120
TTTGGAAAGC CTAGGCCCTC TCCTTGAACC TGGTTCTCAA GGTTTCGGTG ATGAGTCACC 180
TCGTTCCCCC TCACCAGCTT CTGTCTTTAG CCACAGCACT GACGTGTCTG AACCCGCACG 240
CACCTCCTGA GCTGGAGCAC CCGTCATCTT CACACCACAG ATGACTAACC ATGGCCTGCT 300
CACAGTCTCC TCATTATCAC GGAATGAAAA TGCTACATGC CTGAAAGCTG AGGTTTTGGG 360
AACAGGATGA GAAGAGCTGC GGAAGGAATG GAGATGCAGG TGGCAATGAG CTAAGCTTTT 420
GACAGGCCCT CGCAGTCCTC GGGAGCAGGG GCCAAGTGAC CACAGATCCA GAGAGAGTGC 480
TCTCCTTGGC AGGGCCGCAT GAAATCTCAT TCATTACAGC CTCCGATTAG GTTCCCAGGC 540
TCATTAAAAT CTGTGTGCCA TTCACTGTTT CTCTTGGATC AGACTGGATT CTACTGTGCA 600
GAGAATTGCC AGGGCTTCCA AGTGTCCAGT GCAGGCCAGA TAGCATCTCT TGGCTTCACT 660
TCTTCCTGAA GTTTCTCCCT GTGCTTCTGT GTGCTCACTG CCAAGAACAC AAGTCAGCAT 720
TCAGGCCCAC GGCTGCCAGC TGAAACAAGG GCTTCTGACC CAGACAAAGC CCGCAGATAA 780
AGTCCAAAGC ACTTGAGCTA AACTTACTCT AAAAACTATG GCAGTACAGG ACAAAGGAAG 840
ACACTCGGGT TAGACACAAA GAACCACAGC TAAGGCAACC TTTAAAAAAG GAGAGTGGGC 900
TGGGCGCAGT GGCTCATGCC TGTAATCCCA GCACTTTGGG AGGCCAAGGT GGGCGGATCA 960
CTTGAGCTCA 970
|
