Variant report

Variant	rs2322628
Chromosome Location	chr6:80811461-80811462
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1892475	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2256531	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2298307	0.85[ASN][1000 genomes]
rs2322632	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2476826	0.80[EUR][1000 genomes]
rs2490224	0.80[AMR][1000 genomes]
rs2490230	0.80[AMR][1000 genomes]
rs2490232	0.80[AMR][1000 genomes]
rs2490234	0.87[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs2490239	0.87[AFR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2490241	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2505927	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2505929	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2505932	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2505935	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2505939	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2505940	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4706113	0.81[ASN][1000 genomes]
rs56706046	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:80809600-80815800	Weak transcription	Aorta	Aorta
2	chr6:80810400-80815400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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