Variant report

Variant	rs1120673
Chromosome Location	chr3:94683716-94683717
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs1017370	0.97[ASN][1000 genomes]
rs10804440	0.97[ASN][1000 genomes]
rs10804441	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10933818	0.88[ASN][1000 genomes]
rs1120672	0.97[ASN][1000 genomes]
rs11706789	0.97[ASN][1000 genomes]
rs11710300	0.97[ASN][1000 genomes]
rs11718955	0.97[ASN][1000 genomes]
rs11719000	0.98[ASN][1000 genomes]
rs11720623	0.82[ASN][1000 genomes]
rs11918258	0.97[ASN][1000 genomes]
rs11919926	0.91[ASN][1000 genomes]
rs12636346	0.81[AFR][1000 genomes]
rs13072890	0.89[AFR][1000 genomes]
rs1368193	0.97[ASN][1000 genomes]
rs1432468	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1432469	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1432472	0.82[EUR][1000 genomes]
rs1432473	0.97[ASN][1000 genomes]
rs1529652	0.97[ASN][1000 genomes]
rs1529653	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1529654	0.97[ASN][1000 genomes]
rs1549860	0.92[ASN][1000 genomes]
rs1549861	0.90[AFR][1000 genomes]
rs1835872	0.98[ASN][1000 genomes]
rs1897461	0.97[ASN][1000 genomes]
rs1991752	0.91[ASN][1000 genomes]
rs1991753	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2116610	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2116611	0.97[ASN][1000 genomes]
rs2370168	0.89[ASN][1000 genomes]
rs28588046	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs300090	0.88[ASN][1000 genomes]
rs300301	0.95[ASN][1000 genomes]
rs300305	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs300306	0.94[ASN][1000 genomes]
rs380053	0.88[ASN][1000 genomes]
rs4857128	0.90[ASN][1000 genomes]
rs4857129	0.97[ASN][1000 genomes]
rs4857495	0.82[EUR][1000 genomes]
rs49698	0.95[ASN][1000 genomes]
rs6437515	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6807717	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs728066	0.85[ASN][1000 genomes]
rs7622398	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7625912	0.92[ASN][1000 genomes]
rs7626615	0.92[ASN][1000 genomes]
rs7626749	0.97[ASN][1000 genomes]
rs7627012	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9809325	0.97[ASN][1000 genomes]
rs9822197	0.98[ASN][1000 genomes]
rs9822600	0.97[ASN][1000 genomes]
rs9857434	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9861234	0.97[ASN][1000 genomes]
rs9861368	0.86[ASN][1000 genomes]
rs9871759	0.81[AFR][1000 genomes]
rs9880324	0.97[ASN][1000 genomes]
rs991552	0.97[ASN][1000 genomes]
rs997528	0.89[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	nsv877169	chr3:94675697-94840854	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:94683200-94685200	Weak transcription	Fetal Heart	heart

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