Variant report

Variant	rs72661442
Chromosome Location	chr8:60872680-60872681
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10081579	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10087623	0.84[EUR][1000 genomes]
rs10097767	0.90[ASN][1000 genomes]
rs10098915	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10957118	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16925420	0.84[EUR][1000 genomes]
rs17271634	0.95[ASN][1000 genomes]
rs1995941	0.90[ASN][1000 genomes]
rs28445557	0.90[ASN][1000 genomes]
rs28626870	0.90[ASN][1000 genomes]
rs28668089	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28673143	0.95[ASN][1000 genomes]
rs28690268	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55827533	0.84[EUR][1000 genomes]
rs57344747	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62512089	1.00[ASN][1000 genomes]
rs6997337	0.92[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6998079	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72659716	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72659731	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72659733	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72659760	0.85[AFR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72659762	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72659763	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72659765	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72659799	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72659801	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72659802	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72661403	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72661404	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72661406	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72661410	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72661416	0.92[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72661421	0.92[AFR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72661426	0.92[AFR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72661427	0.92[AFR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72661445	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72661495	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72663207	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72663214	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72663216	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72663217	0.85[AMR][1000 genomes]
rs72663221	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72663222	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72663223	0.84[AFR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7833035	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7833043	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7834199	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7837331	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7838137	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9650196	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][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	nsv831331	chr8:60770382-60959633	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:60871600-60884800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr8:60872000-60873200	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr8:60872200-60872800	Enhancers	H9 Cell Line	embryonic stem cell
4	chr8:60872200-60872800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr8:60872400-60872800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr8:60872400-60873000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr8:60872600-60873600	Enhancers	GM12878-XiMat	blood
8	chr8:60872600-60874800	Enhancers	Primary B cells from peripheral blood	blood

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