Variant report

Variant	rs16828819
Chromosome Location	chr3:177668034-177668035
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:49)

rs_ID	r²[population]
rs1075544	0.81[ASN][1000 genomes]
rs10936960	0.81[ASN][1000 genomes]
rs11919677	0.81[ASN][1000 genomes]
rs11920776	0.84[ASN][1000 genomes]
rs11922170	0.84[ASN][1000 genomes]
rs12489750	0.95[ASN][1000 genomes]
rs12492069	0.80[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12492409	0.95[ASN][1000 genomes]
rs12497387	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13062823	0.95[ASN][1000 genomes]
rs13066104	0.81[ASN][1000 genomes]
rs13074448	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13075342	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13087011	0.80[ASN][1000 genomes]
rs13314585	0.80[ASN][1000 genomes]
rs1421157	0.81[ASN][1000 genomes]
rs1421158	0.81[ASN][1000 genomes]
rs1421160	0.81[ASN][1000 genomes]
rs1421161	0.81[ASN][1000 genomes]
rs1421162	0.81[ASN][1000 genomes]
rs1421163	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1421164	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1421169	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1421170	0.82[ASN][1000 genomes]
rs1421173	0.81[ASN][1000 genomes]
rs1582399	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16828811	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1861886	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1895068	0.81[ASN][1000 genomes]
rs34300091	0.82[ASN][1000 genomes]
rs34534264	0.95[ASN][1000 genomes]
rs34603970	0.87[EUR][1000 genomes]
rs34969108	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35494413	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35569214	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35751119	0.97[ASN][1000 genomes]
rs3978728	0.96[ASN][1000 genomes]
rs57315928	0.81[ASN][1000 genomes]
rs6769109	0.81[ASN][1000 genomes]
rs6786110	0.81[ASN][1000 genomes]
rs6804905	0.81[ASN][1000 genomes]
rs737553	0.81[ASN][1000 genomes]
rs737555	0.80[ASN][1000 genomes]
rs7616735	0.86[ASN][1000 genomes]
rs7619802	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7645977	0.82[ASN][1000 genomes]
rs9838142	0.81[ASN][1000 genomes]
rs9862300	0.81[ASN][1000 genomes]
rs9875424	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931055	chr3:177229521-177889872	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv829805	chr3:177662113-177805003	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv997975	chr3:177664921-177719623	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:177666600-177668400	Enhancers	Primary B cells from peripheral blood	blood

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