Variant report

Variant	rs491796
Chromosome Location	chr3:118122723-118122724
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1850944	0.85[ASN][1000 genomes]
rs480491	0.94[ASN][1000 genomes]
rs495761	0.92[ASN][1000 genomes]
rs497009	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs506192	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs507145	0.92[ASN][1000 genomes]
rs508870	0.94[ASN][1000 genomes]
rs518882	0.92[ASN][1000 genomes]
rs523712	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs531289	0.92[ASN][1000 genomes]
rs557455	0.87[ASN][1000 genomes]
rs566574	0.85[ASN][1000 genomes]
rs576638	0.91[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118120000-118128800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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