Variant report

Variant	rs12674936
Chromosome Location	chr8:64768022-64768023
allele	A/C
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]
rs11777464	0.97[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12675356	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12682101	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1356988	1.00[ASN][1000 genomes]
rs1520922	0.81[AMR][1000 genomes]
rs16919009	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17217477	1.00[ASN][1000 genomes]
rs17217512	0.93[AMR][1000 genomes]
rs35972236	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7465464	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7829551	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7832628	0.87[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64768000-64768400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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