| Tag | Content |
|---|
EnhancerAtlas ID | HS184-05897 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:70058240-70059040 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr11:70058567-70058584 | TGAGTTCCTTGCAAGCA | - | 6 | | IRF1 | MA0050.2 | chr11:70058634-70058655 | TTCAGCTTTCACTTTTGGTTG | + | 6.32 | | ZNF263 | MA0528.1 | chr11:70058260-70058281 | CACCCCCTCCCACCCTCCCCC | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 70058304 | 70059000 | | chr11 | 70058385 | 70058983 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I070212 | chr11 | 70058144 | 70059155 |
|
Enhancer Sequence | CCACAGCAAG ACTGTCACCT CACCCCCTCC CACCCTCCCC CGCAGCCCTT GCCCCTGCTG 60
TTTCCTCTCC CTGCAGCCTT CCTCACTATC CACCCCAAGC CCCCCAGCTC AGAAGACATC 120
CTTCTGATGC AGGCTTGCCC ATGCACCCAC TCACAGTGGG ATCCCTGCAG CCCCCACTCC 180
TGCCCGGGTC CTGCTTCCTC TAGCGCGACT CCCTGAGGGC TGCTTCCAGC ACTTTCCAGC 240
GGCTTCTGAG TGAAGGCTTA TTTTGTGTTT GCTGAGTGAA TGAGTAAACA GCAGCGATCA 300
AAGGCCCACT AGCGTCTCTC AGGGGCCTGA GTTCCTTGCA AGCAGGAAAG CAAAAGATGC 360
CTCCGCCCCA GGGTTTCAGA TTCCTGGATT CCCCTTCAGC TTTCACTTTT GGTTGGGCTT 420
CCCAGCCCAG TCAGTCGGAC TGTGAAAGCA CCTGCCCCGC AGTAGGCACG GGCAGGGCAA 480
GAGGGCATCT TCTCAGGGGA GCCAGGTATG CCCCTTGGTC TGCCACCCAT GCATCATATG 540
CCCCTGTTCC CTGAGCCTCT GCTCCCCGCC CCTGGTCCAC ATACCCCCGC CCCGGTGCCC 600
TTCACTCTGA CCAGGCCCAG TGAGCTCCAG CCAGGAACCC CAGGGAGGAG TCCCCACCAC 660
CTGAGTCACT GCAGGCCATC CCAGGGGTCC TACTCGCCAG GAAGGGTTGA CGCCCACGTA 720
CACATACACC TCTGGGCTCC TGGCACTCTG AGCTGTATGT TTCATTCTGG TTCATTCACC 780
ATTCATTCAT TTACTCGGTA 800
|
