| Tag | Content |
|---|
EnhancerAtlas ID | HS184-11034 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr15:40566650-40567370 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr15:40567040-40567059 | GGACGCCCCCTGCTGGCAG | - | 6.48 | | CTCF | MA0139.1 | chr15:40567082-40567101 | CACCGCCATCTGGTGGCCA | - | 8.63 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH15I040274 | chr15 | 40566801 | 40567401 |
|
Enhancer Sequence | GCACAAGTTC GCATGTGCGC TCCGACAAGT CGCCTCCCAC GGCTGTGGCA GGAGAGTTGC 60
TGCTTGGCAG AAGGGTTGCT GCTTGGCAGG CACTGGTCGG AAGCCCAGTG GGGCCCATGA 120
GCAGGGAAAG CCAGGACACC AGCAATCCCT GCTGTCCAGG GAGGGATCCG GAGAAGCTTC 180
ACTGAGCACA AACCCTTCTA ACCCGTGTCG GGAGATCCAT ACCATGATTC GATGTCCCTG 240
TCCATCACGG CGAGTCGGCT CATGCTCCAT CGTTGCACAC CCCGACACAG CTAAGCCACA 300
GCGTTCCCCT TAAAGCCAGT ATAAGTGCAT GGAAGTGTAT ACATGTAACC CTTTTTGCCA 360
AATCGGCCCC AACCCCGCAG GCCTTACTGT GGACGCCCCC TGCTGGCAGG TCAGCACGGG 420
GCTGCTAAGT GGCACCGCCA TCTGGTGGCC AAAACAAGAA ATGTCTCAGA GGGCTGAAGC 480
CTCTCCTCTA AAATAGCAAA AAAACAAGAG TTCTGTGGCC CCAACACAAA GCTGGATGGG 540
AGGACCAACA GGAAACATCT TCCAAGACAA CTGGTCCTTG GAGCCCGCAC CGCTAACCCC 600
AAAATTAGCA TATAAAGATC TCCAGTTGGC TAATTCCTCA GAGGATGTAG CCTTCTGCCC 660
AAGACTCAGC CTCATCCCAA GATACTGGCT CAAAATGAAC CAAGATAAGC CCTTGCTTTA 720
|
