The 2.0 version of rSNPBase
Home
Search
Document
What's New
Tutorial
Data Content
Download
Feedback
About Us
Variant report
Variant
rs7295914
Chromosome Location
chr12:75045595-75045596
allele
C/T
Outlinks
Ensembl
 
UCSC
Chromatin state
Related regulatory elements
Target genes
Other information
TF binding region (count:0)
CpG islands (count:0)
Chromatin interactive region (count:1)
LncRNA region (count:0)
Mature miRNA region (count: 0)
miRNA target sites (count:0)
No data
No data
(count:1 , 50 per page) page:
1
No.
Distal block
Cell Line
Cell type
Cell Stage
1
chr12:74930398..74932060-chr12:75044230..75046232,2
MCF-7
breast:
No data
No data
No data
Variant related genes
Relation type
ENSG00000253719
Chromatin interaction
Extended variants information (count: 8 )
Associated traits (count: 0)
rSNPs within LD-proxies of this variant (count:8)
rs_ID
r
2
[population]
rs17113755
0.85[YRI][hapmap]
rs7299112
0.88[YRI][hapmap]
rs7299181
1.00[LWK][hapmap];0.93[YRI][hapmap];0.95[AFR][1000 genomes]
rs7308545
0.90[AFR][1000 genomes]
rs74106013
0.93[AFR][1000 genomes]
rs74106017
0.88[AFR][1000 genomes]
rs74106055
0.93[AFR][1000 genomes]
rs7973277
0.93[YRI][hapmap]
No data
Chromatin state (count:0 , 50 per page) page:
No data
Quick Search:
Input of quick search could be:
dbSNP/dbVar ID:
rs12345
/
nsv7879
a single nucleotide as 0-based coordinates:
chr1:12345
chromosomal regions:
chr1:12345-34567
what's new
New variant types
New dimension of annotation
New regulatory manner
More detailed annotation on variant overlapped TFBS
More extended data
New search manner
Quick links