Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:181730611..181732422-chr2:181735699..181737435,2	K562	blood:

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10178270	0.90[ASN][1000 genomes]
rs10189224	0.91[ASN][1000 genomes]
rs11894079	0.99[ASN][1000 genomes]
rs12328545	0.90[ASN][1000 genomes]
rs12471143	0.96[ASN][1000 genomes]
rs12619585	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13387820	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13426990	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3922471	0.90[ASN][1000 genomes]
rs3922472	0.88[ASN][1000 genomes]
rs4128869	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs4128870	0.96[ASN][1000 genomes]
rs4290619	0.90[ASN][1000 genomes]
rs4315481	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs4359601	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4436925	0.93[ASN][1000 genomes]
rs4666608	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4666643	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4666946	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4666957	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62178176	0.80[ASN][1000 genomes]
rs62178210	0.91[ASN][1000 genomes]
rs62178239	0.90[ASN][1000 genomes]
rs62178240	0.90[ASN][1000 genomes]
rs6724902	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6730421	0.93[ASN][1000 genomes]
rs6734821	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6756832	0.99[ASN][1000 genomes]
rs9677524	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[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	nsv963752	chr2:181734234-181756646	Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:181736400-181737000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr2:181736400-181737200	Enhancers	NHDF-Ad	bronchial
3	chr2:181736400-181738200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr2:181736600-181737000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:181736600-181737000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
6	chr2:181736600-181737200	Enhancers	HSMMtube	muscle
7	chr2:181736600-181737200	Enhancers	NHLF	lung

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