Variant report

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

rs_ID	r²[population]
rs10004804	0.91[ASN][1000 genomes]
rs10856919	0.90[ASN][1000 genomes]
rs11097501	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12499067	0.86[ASN][1000 genomes]
rs12642621	0.81[ASN][1000 genomes]
rs13121458	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13122821	0.83[ASN][1000 genomes]
rs13122856	0.81[ASN][1000 genomes]
rs1373331	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1425361	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1444021	0.83[ASN][1000 genomes]
rs1506317	0.81[ASN][1000 genomes]
rs1506321	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1834360	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1847968	0.81[ASN][1000 genomes]
rs1857890	0.82[ASN][1000 genomes]
rs1867400	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2197322	0.81[ASN][1000 genomes]
rs4699483	0.83[ASN][1000 genomes]
rs4699485	0.86[ASN][1000 genomes]
rs6532596	0.86[ASN][1000 genomes]
rs6532597	0.86[ASN][1000 genomes]
rs6815743	0.81[ASN][1000 genomes]
rs6826156	0.86[ASN][1000 genomes]
rs6826817	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7665151	0.86[ASN][1000 genomes]
rs7671563	0.85[ASN][1000 genomes]
rs7676317	0.86[ASN][1000 genomes]
rs7676764	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830013	chr4:97033125-97204291	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1003868	chr4:97068155-97222544	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:97083600-97088200	Enhancers	Osteobl	bone
2	chr4:97085800-97087800	Enhancers	HSMMtube	muscle
3	chr4:97085800-97088200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr4:97085800-97088400	Enhancers	Muscle Satellite Cultured Cells	--
5	chr4:97086600-97088400	Enhancers	HSMM	muscle

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