Variant report

Variant	rs2326913
Chromosome Location	chr6:130888051-130888052
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs12665689	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1316493	0.91[ASN][1000 genomes]
rs1316537	0.91[ASN][1000 genomes]
rs1316538	0.91[ASN][1000 genomes]
rs1317232	0.91[ASN][1000 genomes]
rs17059212	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1815602	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1933757	0.91[ASN][1000 genomes]
rs2209147	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4895886	0.92[ASN][1000 genomes]
rs4895887	0.87[ASN][1000 genomes]
rs4895888	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4897437	0.91[ASN][1000 genomes]
rs4897438	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4897439	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56019502	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62431563	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62431565	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62431566	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6569690	0.91[ASN][1000 genomes]
rs6899678	0.92[ASN][1000 genomes]
rs6932512	0.91[ASN][1000 genomes]
rs72988212	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7451336	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7452034	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7744825	0.91[ASN][1000 genomes]
rs7754423	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9321238	0.92[ASN][1000 genomes]
rs9321239	0.92[ASN][1000 genomes]
rs9321241	0.92[ASN][1000 genomes]
rs9372966	0.91[ASN][1000 genomes]
rs9372967	0.90[ASN][1000 genomes]
rs9375727	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9375740	0.91[ASN][1000 genomes]
rs9375741	0.91[ASN][1000 genomes]
rs9385545	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9385546	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9402246	0.87[ASN][1000 genomes]
rs9402247	0.91[ASN][1000 genomes]
rs9402248	0.91[ASN][1000 genomes]
rs9483145	0.92[ASN][1000 genomes]
rs9492649	0.91[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	nsv533971	chr6:130490694-131172051	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv427767	chr6:130875056-131008620	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv5475	chr6:130880169-130924850	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	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	chr6:130882600-130894400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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