Variant report

Variant	rs10503963
Chromosome Location	chr8:34340682-34340683
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16882098	0.95[AMR][1000 genomes]
rs16882394	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs16882469	0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16882472	0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16882616	0.84[AMR][1000 genomes]
rs16882698	0.84[AMR][1000 genomes]
rs4739575	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4739576	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4739577	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4739578	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4739579	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4739588	0.90[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6997049	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv6147	chr8:34314029-34359124	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34340200-34343800	Weak transcription	Fetal Kidney	kidney

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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