Variant report

Variant	rs7092910
Chromosome Location	chr10:22796761-22796762
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11599280	0.95[CEU][hapmap];0.95[CHB][hapmap];0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs12221321	0.97[ASN][1000 genomes]
rs12767557	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12770182	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs35354362	0.94[ASN][1000 genomes]
rs4590763	0.80[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap];0.85[ASN][1000 genomes]
rs61847436	0.94[ASN][1000 genomes]
rs7478665	0.81[EUR][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:22765800-22806600	Weak transcription	Right Atrium	heart
2	chr10:22793000-22797000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr10:22794000-22796800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
4	chr10:22795200-22796800	Enhancers	Primary T helper naive cells fromperipheralblood	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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