Variant report

Variant	rs60856949
Chromosome Location	chr5:36508477-36508478
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10053299	1.00[EUR][1000 genomes]
rs10054009	1.00[EUR][1000 genomes]
rs10056349	1.00[EUR][1000 genomes]
rs10056352	1.00[EUR][1000 genomes]
rs10056466	1.00[EUR][1000 genomes]
rs10058111	1.00[EUR][1000 genomes]
rs10058115	1.00[EUR][1000 genomes]
rs10058314	1.00[EUR][1000 genomes]
rs10058422	1.00[EUR][1000 genomes]
rs10058564	1.00[EUR][1000 genomes]
rs10061999	1.00[EUR][1000 genomes]
rs10073164	1.00[EUR][1000 genomes]
rs10073279	1.00[EUR][1000 genomes]
rs10077206	1.00[EUR][1000 genomes]
rs10077918	1.00[EUR][1000 genomes]
rs10079668	1.00[EUR][1000 genomes]
rs10085047	1.00[EUR][1000 genomes]
rs10085102	1.00[EUR][1000 genomes]
rs11954566	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13354988	1.00[EUR][1000 genomes]
rs16903262	1.00[AMR][1000 genomes]
rs28376702	1.00[EUR][1000 genomes]
rs28479598	1.00[EUR][1000 genomes]
rs28505610	1.00[EUR][1000 genomes]
rs28523559	1.00[EUR][1000 genomes]
rs28647761	1.00[EUR][1000 genomes]
rs56288606	1.00[EUR][1000 genomes]
rs57097362	1.00[EUR][1000 genomes]
rs57336573	1.00[EUR][1000 genomes]
rs58556892	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59457338	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60250007	1.00[AMR][1000 genomes]
rs60852665	1.00[AMR][1000 genomes]
rs61246645	1.00[EUR][1000 genomes]
rs61448540	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6861244	1.00[AMR][1000 genomes]
rs6890988	1.00[AMR][1000 genomes]
rs73089639	1.00[AMR][1000 genomes]
rs73089649	1.00[AMR][1000 genomes]
rs73089650	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73089652	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73089653	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73089661	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73089667	1.00[EUR][1000 genomes]
rs73089669	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73089699	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73089701	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73091531	1.00[AMR][1000 genomes]
rs7703416	1.00[AMR][1000 genomes]
rs7703852	1.00[AMR][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	nsv881666	chr5:36498183-36537369	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36507200-36508600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr5:36508200-36508600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr5:36508400-36508600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:36508400-36508600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:36508400-36508600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr5:36508400-36508800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:36508400-36509000	Enhancers	Right Ventricle	heart

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