Variant report

Variant	rs7192050
Chromosome Location	chr16:64771286-64771287
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11859763	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11862881	0.88[ASN][1000 genomes]
rs12446839	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12597618	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12919603	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1423987	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1423988	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1423997	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs179522	0.96[ASN][1000 genomes]
rs2107370	0.83[ASN][1000 genomes]
rs231034	0.95[ASN][1000 genomes]
rs231035	0.95[ASN][1000 genomes]
rs231037	0.95[ASN][1000 genomes]
rs231076	0.93[ASN][1000 genomes]
rs231078	0.93[ASN][1000 genomes]
rs231089	0.89[ASN][1000 genomes]
rs231091	0.89[ASN][1000 genomes]
rs231097	0.90[ASN][1000 genomes]
rs231104	0.90[ASN][1000 genomes]
rs231106	0.89[ASN][1000 genomes]
rs231111	0.90[ASN][1000 genomes]
rs2320127	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4967867	0.84[ASN][1000 genomes]
rs55840743	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6498959	0.87[ASN][1000 genomes]
rs6498961	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7185558	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7190938	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7200356	0.87[ASN][1000 genomes]
rs7200661	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7206276	0.86[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	nsv984341	chr16:64770082-64771386	Weak transcription Enhancers	TF binding region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:64767600-64772200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr16:64771200-64772400	Weak transcription	Osteobl	bone

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