Variant report

Variant	rs7920590
Chromosome Location	chr10:93156076-93156077
allele	A/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]
rs11186548	0.87[EUR][1000 genomes]
rs12244852	0.80[EUR][1000 genomes]
rs12248059	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12257543	0.80[EUR][1000 genomes]
rs12266111	0.80[EUR][1000 genomes]
rs17106706	0.80[EUR][1000 genomes]
rs6583771	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7071064	0.80[EUR][1000 genomes]
rs7081299	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7081707	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7087338	0.80[EUR][1000 genomes]
rs7894994	0.87[EUR][1000 genomes]
rs7903943	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93150000-93156800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr10:93155400-93156200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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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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