Variant report

Variant	rs6821676
Chromosome Location	chr4:81346212-81346213
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:81336924..81338825-chr4:81344447..81347263,2	K562	blood:

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10031438	0.90[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1039054	0.87[ASN][1000 genomes]
rs11099227	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11099231	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11099233	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11099236	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11099238	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1156872	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11721676	0.87[ASN][1000 genomes]
rs11723594	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11724838	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11727411	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11729082	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11731757	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11736014	0.82[AFR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11736601	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11929913	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11930816	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11932267	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11936436	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11936703	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11938178	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11939741	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11944059	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11946412	0.87[ASN][1000 genomes]
rs12501575	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13108814	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13129145	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1390254	0.86[ASN][1000 genomes]
rs1458026	0.84[CHB][hapmap]
rs1458045	0.89[CHB][hapmap]
rs17004891	0.83[ASN][1000 genomes]
rs17004906	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1994981	0.84[ASN][1000 genomes]
rs1994982	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2047235	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2201531	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28463662	0.85[ASN][1000 genomes]
rs4693022	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs55912262	0.85[EUR][1000 genomes]
rs56054570	0.87[ASN][1000 genomes]
rs56267604	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs57025153	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs57686880	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60513752	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60554077	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61325136	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6534957	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6821990	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6842892	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72860771	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72860772	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72860777	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72860781	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72860789	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72860798	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72862015	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7654257	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7670914	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7695356	0.82[AFR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7699572	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9307683	0.88[AFR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9990885	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999334	chr4:81324288-81409040	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv537153	chr4:81324288-81409040	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:81345200-81346800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr4:81345600-81346800	Enhancers	K562	blood
3	chr4:81345600-81348800	Enhancers	Brain Germinal Matrix	brain

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