Variant report

Variant	rs73267740
Chromosome Location	chr12:41065825-41065826
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs1013929	0.85[ASN][1000 genomes]
rs10161138	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10161509	0.80[ASN][1000 genomes]
rs10735957	0.85[ASN][1000 genomes]
rs10748138	0.87[ASN][1000 genomes]
rs10748148	0.82[ASN][1000 genomes]
rs10784796	0.85[ASN][1000 genomes]
rs10784797	0.82[ASN][1000 genomes]
rs10784800	0.85[ASN][1000 genomes]
rs10879028	0.82[AMR][1000 genomes]
rs10879031	0.80[ASN][1000 genomes]
rs10879079	0.82[AMR][1000 genomes]
rs10879092	0.82[ASN][1000 genomes]
rs10879095	0.80[ASN][1000 genomes]
rs11177589	0.82[EUR][1000 genomes]
rs11177809	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11177862	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11177863	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11177886	0.82[AMR][1000 genomes]
rs11177927	0.82[AMR][1000 genomes]
rs11178000	0.82[AMR][1000 genomes]
rs11178013	0.82[AMR][1000 genomes]
rs11178015	0.82[AMR][1000 genomes]
rs11178017	0.82[AMR][1000 genomes]
rs11178018	0.82[AMR][1000 genomes]
rs11178027	0.82[AMR][1000 genomes]
rs11178050	0.80[AMR][1000 genomes]
rs11178067	0.82[ASN][1000 genomes]
rs11178070	0.82[AMR][1000 genomes]
rs11178118	0.82[AMR][1000 genomes]
rs11178122	0.82[AMR][1000 genomes]
rs12296967	0.80[ASN][1000 genomes]
rs12367287	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12367641	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12372385	0.82[AMR][1000 genomes]
rs1373425	0.85[ASN][1000 genomes]
rs1373426	0.85[ASN][1000 genomes]
rs1584094	0.80[ASN][1000 genomes]
rs1584095	0.85[ASN][1000 genomes]
rs1918951	0.80[ASN][1000 genomes]
rs1918953	0.81[EUR][1000 genomes]
rs1992606	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2405290	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2405293	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2405294	0.85[ASN][1000 genomes]
rs3940638	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61915074	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61915099	0.82[AMR][1000 genomes]
rs61915100	0.82[AMR][1000 genomes]
rs61915101	0.82[AMR][1000 genomes]
rs61915102	0.82[AMR][1000 genomes]
rs7133642	0.82[ASN][1000 genomes]
rs7139243	0.82[AMR][1000 genomes]
rs7311914	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7312935	0.82[AMR][1000 genomes]
rs7953546	0.85[ASN][1000 genomes]
rs7960217	0.82[AMR][1000 genomes]
rs7962501	0.85[ASN][1000 genomes]
rs7972371	0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7974939	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs935224	0.92[ASN][1000 genomes]
rs9669757	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9783468	0.83[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	nsv899033	chr12:40758652-41122288	Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv832378	chr12:40943111-41132305	Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv427909	chr12:41054306-41322257	Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv832379	chr12:41054440-41232749	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs73267740	CNTN1	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41062600-41066600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr12:41062800-41066600	Weak transcription	Fetal Kidney	kidney
3	chr12:41064200-41066000	Weak transcription	Fetal Lung	lung
4	chr12:41065800-41067400	Enhancers	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links