Variant report

Variant	rs57995155
Chromosome Location	chr8:91494609-91494610
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs57350729	0.86[AFR][1000 genomes]
rs57550344	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57820529	1.00[AMR][1000 genomes]
rs57982498	1.00[AMR][1000 genomes]
rs59588987	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61305476	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61504138	0.86[AFR][1000 genomes]
rs73303917	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303921	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303924	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303926	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303930	1.00[AFR][1000 genomes]
rs73303944	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303958	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303965	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303968	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303972	1.00[AMR][1000 genomes]
rs73303973	1.00[AMR][1000 genomes]
rs73303974	1.00[AMR][1000 genomes]
rs73303980	1.00[AMR][1000 genomes]
rs73303981	1.00[AMR][1000 genomes]
rs73303984	1.00[AMR][1000 genomes]
rs73303987	1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91491800-91495400	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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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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