Variant report

Variant	rs1781939
Chromosome Location	chr10:5201979-5201980
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 138 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:113)

rs_ID	r²[population]
rs10752001	0.83[CHB][hapmap]
rs10752005	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs10795242	0.83[CHB][hapmap]
rs10795245	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs10904432	1.00[ASN][1000 genomes]
rs11252922	0.83[CHB][hapmap]
rs11253024	1.00[ASN][1000 genomes]
rs11492967	1.00[ASN][1000 genomes]
rs11511661	1.00[ASN][1000 genomes]
rs11511664	1.00[ASN][1000 genomes]
rs11524375	1.00[ASN][1000 genomes]
rs1155931	1.00[ASN][1000 genomes]
rs12355837	1.00[ASN][1000 genomes]
rs12355966	0.97[ASN][1000 genomes]
rs12356304	1.00[ASN][1000 genomes]
rs12387	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs12529	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs12775468	0.80[ASN][1000 genomes]
rs12775701	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs17134471	0.91[CHB][hapmap];1.00[JPT][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1761601	1.00[ASN][1000 genomes]
rs1761602	1.00[ASN][1000 genomes]
rs1761603	0.98[ASN][1000 genomes]
rs1761604	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1761606	1.00[ASN][1000 genomes]
rs1781927	0.94[ASN][1000 genomes]
rs1781929	0.98[ASN][1000 genomes]
rs1781930	0.98[ASN][1000 genomes]
rs1781932	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1781933	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1781935	1.00[ASN][1000 genomes]
rs1781937	1.00[ASN][1000 genomes]
rs1781938	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1781940	1.00[ASN][1000 genomes]
rs1781941	0.94[ASN][1000 genomes]
rs1892404	0.80[ASN][1000 genomes]
rs1937840	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs1937841	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs1937845	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs1937847	0.91[CHB][hapmap]
rs1937848	0.91[CHB][hapmap]
rs1937849	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs1937882	0.85[ASN][1000 genomes]
rs1937916	0.90[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs2151899	0.91[ASN][1000 genomes]
rs2151900	0.97[ASN][1000 genomes]
rs2154308	0.85[ASN][1000 genomes]
rs2186175	0.85[ASN][1000 genomes]
rs2211630	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs2226260	0.80[ASN][1000 genomes]
rs2298305	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs2398103	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2398195	0.80[ASN][1000 genomes]
rs2398196	0.91[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs2518047	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs2518049	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs2801882	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs2801883	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs34573009	0.95[ASN][1000 genomes]
rs34606065	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3750573	0.91[CHB][hapmap];1.00[JPT][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4242785	0.91[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes]
rs4330990	0.98[ASN][1000 genomes]
rs4494227	0.91[ASN][1000 genomes]
rs4622159	0.80[ASN][1000 genomes]
rs4880708	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs4880710	0.91[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs4881395	0.81[CHB][hapmap]
rs4881396	0.83[CHB][hapmap]
rs4881397	0.83[CHB][hapmap]
rs4881403	0.83[ASN][1000 genomes]
rs4881404	0.91[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs4881408	1.00[ASN][1000 genomes]
rs4881410	1.00[ASN][1000 genomes]
rs56312472	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs57097292	0.85[AFR][1000 genomes]
rs60878270	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61854684	0.98[ASN][1000 genomes]
rs61854686	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61854687	0.98[ASN][1000 genomes]
rs61854697	0.98[ASN][1000 genomes]
rs61854701	0.95[ASN][1000 genomes]
rs61854702	0.95[ASN][1000 genomes]
rs61854705	0.95[ASN][1000 genomes]
rs6601898	0.83[CHB][hapmap]
rs6601899	0.83[CHB][hapmap]
rs6601919	1.00[ASN][1000 genomes]
rs6601920	1.00[ASN][1000 genomes]
rs6601921	1.00[ASN][1000 genomes]
rs6601923	1.00[ASN][1000 genomes]
rs7067921	0.91[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7070300	1.00[ASN][1000 genomes]
rs7071406	1.00[ASN][1000 genomes]
rs7072048	0.97[ASN][1000 genomes]
rs7072750	1.00[ASN][1000 genomes]
rs7074118	0.85[ASN][1000 genomes]
rs7080497	1.00[ASN][1000 genomes]
rs7084630	0.89[ASN][1000 genomes]
rs7086984	0.80[ASN][1000 genomes]
rs7089964	1.00[ASN][1000 genomes]
rs7090038	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72478267	0.92[ASN][1000 genomes]
rs7898263	0.83[CHB][hapmap]
rs7898341	1.00[ASN][1000 genomes]
rs7901781	0.83[CHB][hapmap]
rs7902978	1.00[ASN][1000 genomes]
rs7914117	0.80[ASN][1000 genomes]
rs7917079	0.80[ASN][1000 genomes]
rs7918456	1.00[ASN][1000 genomes]
rs7920135	0.80[ASN][1000 genomes]
rs878766	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9731372	0.83[ASN][1000 genomes]
rs9794201	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894792	chr10:4832920-5498724	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv948794	chr10:4863093-5227382	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv1045155	chr10:4872239-5211318	Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv869470	chr10:4878904-5203685	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv466713	chr10:4901798-5319679	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
6	nsv549881	chr10:4901798-5319679	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	nsv534685	chr10:4914018-5853324	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
8	nsv1050246	chr10:4927428-5211318	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
9	nsv549882	chr10:4943518-5203864	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
10	esv2763913	chr10:4961021-5321407	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
11	nsv1039386	chr10:5008383-5348491	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
12	nsv1036566	chr10:5037926-5261426	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
13	nsv549883	chr10:5037926-5275762	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
14	nsv1047484	chr10:5076258-5261482	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
15	nsv1036291	chr10:5076258-5456234	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
16	nsv540465	chr10:5108345-5261482	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
17	nsv540467	chr10:5114577-5225365	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
18	nsv540468	chr10:5114577-5261482	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
19	nsv540469	chr10:5120774-5225365	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
20	nsv540470	chr10:5120774-5261482	Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
21	nsv540471	chr10:5133561-5261482	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
22	nsv540472	chr10:5133561-5284334	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
23	nsv1048081	chr10:5149144-5321395	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
24	esv3387745	chr10:5201939-5324885	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
25	esv3370619	chr10:5201974-5324834	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5194400-5206600	Strong transcription	Liver	Liver
2	chr10:5198000-5202800	Weak transcription	Adipose Nuclei	Adipose
3	chr10:5198200-5207200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr10:5201600-5202000	Enhancers	Monocytes-CD14+_RO01746	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links