Variant report

Variant	rs1360954
Chromosome Location	chr10:97861897-97861898
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs12098340	0.86[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs17111341	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs17111359	1.00[CEU][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17111364	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs17111391	1.00[CEU][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes]
rs56046295	0.95[EUR][1000 genomes]
rs57904662	0.95[EUR][1000 genomes]
rs60064761	0.81[EUR][1000 genomes]
rs60218681	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs7079761	1.00[CEU][hapmap]
rs7081962	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs7087254	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs73320939	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73320962	0.81[EUR][1000 genomes]
rs7900016	0.95[EUR][1000 genomes]
rs7902556	0.95[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97860800-97867200	Weak transcription	K562	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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