Variant report

Variant	rs10111531
Chromosome Location	chr8:91426609-91426610
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10086788	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10087100	0.93[EUR][1000 genomes]
rs10099647	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10100923	0.96[EUR][1000 genomes]
rs10103125	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10103138	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10103492	1.00[CEU][hapmap]
rs10104445	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10104451	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10106274	0.93[EUR][1000 genomes]
rs10112375	0.93[EUR][1000 genomes]
rs10112676	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1015844	0.93[EUR][1000 genomes]
rs10216873	0.93[EUR][1000 genomes]
rs11995911	1.00[CEU][hapmap]
rs11996705	1.00[CEU][hapmap]
rs13439871	0.86[EUR][1000 genomes]
rs16904523	1.00[ASN][1000 genomes]
rs16904545	0.89[EUR][1000 genomes]
rs16904875	1.00[CEU][hapmap]
rs16904876	1.00[CEU][hapmap]
rs28385552	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28550265	0.93[EUR][1000 genomes]
rs28684622	0.93[EUR][1000 genomes]
rs28687302	1.00[ASN][1000 genomes]
rs28715738	1.00[ASN][1000 genomes]
rs28882092	0.93[EUR][1000 genomes]
rs4474067	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4570116	1.00[CEU][hapmap]
rs5005584	1.00[CEU][hapmap]
rs58836045	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72675652	0.86[ASN][1000 genomes]
rs9297838	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv981884	chr8:91420804-91441125	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91395000-91433400	Weak transcription	K562	blood

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