Variant report

Variant	rs2317246
Chromosome Location	chr3:56742582-56742583
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11927033	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2317248	0.82[AMR][1000 genomes]
rs4273342	0.82[AMR][1000 genomes]
rs4407379	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4634082	0.82[AMR][1000 genomes]
rs6445815	0.82[AMR][1000 genomes]
rs6772854	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6805910	0.82[AMR][1000 genomes]
rs6807177	0.82[AMR][1000 genomes]
rs7629016	0.82[AMR][1000 genomes]
rs9813229	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9857253	0.82[AMR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:56734800-56756400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:56739400-56758600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr3:56742200-56753000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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