Variant report

Variant	rs10170897
Chromosome Location	chr2:191251685-191251686
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10190016	0.91[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10202825	0.82[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.95[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10208045	0.82[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs13390311	0.98[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs13409203	0.81[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs16832573	0.90[CHB][hapmap]
rs34121676	0.83[ASN][1000 genomes]
rs36015572	0.82[ASN][1000 genomes]
rs3811610	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs73048070	1.00[ASN][1000 genomes]
rs73050047	0.96[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:191251400-191251800	Enhancers	NHDF-Ad	bronchial

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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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