Variant report

Variant	rs200011
Chromosome Location	chr5:8696317-8696318
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs169239	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs187964	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs199181	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs199997	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs199998	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199999	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs200000	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs200001	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs200002	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs200003	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs200006	0.83[EUR][1000 genomes]
rs200008	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs200009	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs200010	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs200012	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs200013	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs200014	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs200015	0.99[ASN][1000 genomes]
rs200017	0.99[ASN][1000 genomes]
rs200018	0.99[ASN][1000 genomes]
rs200036	0.99[ASN][1000 genomes]
rs200037	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs200038	0.99[ASN][1000 genomes]
rs200039	0.99[ASN][1000 genomes]
rs200040	0.99[ASN][1000 genomes]
rs200043	0.99[ASN][1000 genomes]
rs200044	0.99[ASN][1000 genomes]
rs200046	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs200047	0.99[ASN][1000 genomes]
rs200048	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs200049	0.99[ASN][1000 genomes]
rs200050	0.97[ASN][1000 genomes]
rs200052	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs200053	0.97[ASN][1000 genomes]
rs200064	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs200066	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs200068	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs200069	0.95[ASN][1000 genomes]
rs200095	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2519880	0.99[ASN][1000 genomes]
rs2651645	0.99[ASN][1000 genomes]
rs2963389	0.91[JPT][hapmap]
rs976987	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032346	chr5:8522331-8747061	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv537636	chr5:8522331-8747061	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1033498	chr5:8554438-8702228	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv537637	chr5:8690735-8730509	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	n/a	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	chr5:8693000-8697600	Enhancers	Fetal Lung	lung
2	chr5:8695800-8696800	Enhancers	Fetal Muscle Leg	muscle
3	chr5:8695800-8696800	Enhancers	Fetal Stomach	stomach

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