Variant report

Variant	rs235610
Chromosome Location	chr12:47025942-47025943
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:47025079..47028602-chr12:47029579..47033419,4	MCF-7	breast:

Extended variants
information (count: 152 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:144)

rs_ID	r²[population]
rs10785631	1.00[CEU][hapmap]
rs10880975	1.00[CEU][hapmap]
rs10880976	1.00[CEU][hapmap]
rs10880977	1.00[CEU][hapmap]
rs10880980	0.81[EUR][1000 genomes]
rs11183497	1.00[CEU][hapmap]
rs11183524	0.93[EUR][1000 genomes]
rs11183536	0.93[EUR][1000 genomes]
rs11183539	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11183547	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11183550	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11829502	1.00[CEU][hapmap]
rs11830099	0.88[EUR][1000 genomes]
rs11830501	0.88[EUR][1000 genomes]
rs11831177	1.00[CEU][hapmap]
rs11831920	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs11831929	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs11832316	0.88[EUR][1000 genomes]
rs11833393	0.93[EUR][1000 genomes]
rs11834607	0.93[EUR][1000 genomes]
rs11835517	0.88[EUR][1000 genomes]
rs11835974	0.88[EUR][1000 genomes]
rs11836915	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs11836940	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs11837104	0.88[EUR][1000 genomes]
rs12300125	1.00[CEU][hapmap];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12305921	1.00[CEU][hapmap]
rs12310635	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12320420	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12578813	0.95[EUR][1000 genomes]
rs12579089	0.95[EUR][1000 genomes]
rs12579348	0.88[EUR][1000 genomes]
rs12579976	0.88[EUR][1000 genomes]
rs12580092	0.95[EUR][1000 genomes]
rs12580121	1.00[CEU][hapmap]
rs12580356	0.95[EUR][1000 genomes]
rs12580488	0.91[EUR][1000 genomes]
rs12581205	0.86[EUR][1000 genomes]
rs12581311	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12581366	0.95[EUR][1000 genomes]
rs12582013	0.91[EUR][1000 genomes]
rs12582056	1.00[CEU][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12582305	1.00[CEU][hapmap]
rs12582476	0.95[EUR][1000 genomes]
rs17096991	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs17096995	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs17097002	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs17097009	0.88[EUR][1000 genomes]
rs17097022	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs17121410	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs17121412	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs17594275	0.91[EUR][1000 genomes]
rs17611638	0.95[EUR][1000 genomes]
rs1946175	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2042058	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2193662	0.84[EUR][1000 genomes]
rs2193663	0.88[EUR][1000 genomes]
rs2216439	0.85[EUR][1000 genomes]
rs235600	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs235601	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs235602	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs235607	1.00[CEU][hapmap];0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs235616	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs235617	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs235621	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs235622	1.00[CEU][hapmap];0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs235625	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs235626	1.00[CEU][hapmap];0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs235627	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2408576	0.88[EUR][1000 genomes]
rs2408577	0.93[EUR][1000 genomes]
rs2430937	0.93[EUR][1000 genomes]
rs2430939	0.93[EUR][1000 genomes]
rs2430940	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2430941	0.93[EUR][1000 genomes]
rs2430942	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs2430943	0.93[EUR][1000 genomes]
rs2430946	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs2430947	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs2471581	0.81[EUR][1000 genomes]
rs2471583	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs2471588	0.93[EUR][1000 genomes]
rs2471594	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs2471601	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2471602	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs2471605	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs2471608	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs2471617	0.93[EUR][1000 genomes]
rs2471618	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs28768973	0.93[EUR][1000 genomes]
rs2897969	0.84[EUR][1000 genomes]
rs2909411	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs2960450	0.93[EUR][1000 genomes]
rs34008890	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35096979	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4073924	0.81[EUR][1000 genomes]
rs4604970	0.88[EUR][1000 genomes]
rs4768125	0.86[EUR][1000 genomes]
rs4768741	1.00[CEU][hapmap];0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4768742	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4768744	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56111534	0.93[EUR][1000 genomes]
rs56152575	0.88[EUR][1000 genomes]
rs56181923	0.88[EUR][1000 genomes]
rs56271434	0.88[EUR][1000 genomes]
rs56399247	0.81[EUR][1000 genomes]
rs57158113	0.81[EUR][1000 genomes]
rs57370043	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57658610	0.93[EUR][1000 genomes]
rs58449317	0.88[EUR][1000 genomes]
rs58503088	0.88[EUR][1000 genomes]
rs58561072	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58813899	0.88[EUR][1000 genomes]
rs59903937	0.88[EUR][1000 genomes]
rs60191997	0.93[EUR][1000 genomes]
rs60432604	0.81[EUR][1000 genomes]
rs60669661	0.88[EUR][1000 genomes]
rs60681792	0.88[EUR][1000 genomes]
rs61072098	0.90[EUR][1000 genomes]
rs61355826	0.93[EUR][1000 genomes]
rs61641663	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6582666	1.00[CEU][hapmap]
rs7138914	0.88[EUR][1000 genomes]
rs7295471	1.00[CEU][hapmap]
rs7308386	0.88[EUR][1000 genomes]
rs7310326	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs7310408	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73282109	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73290381	0.81[EUR][1000 genomes]
rs73290402	0.88[EUR][1000 genomes]
rs73291964	0.88[EUR][1000 genomes]
rs73291976	0.88[EUR][1000 genomes]
rs73291980	0.88[EUR][1000 genomes]
rs73292000	0.88[EUR][1000 genomes]
rs73292001	0.93[EUR][1000 genomes]
rs73293911	0.88[EUR][1000 genomes]
rs73293919	0.88[EUR][1000 genomes]
rs7484802	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7488464	0.93[EUR][1000 genomes]
rs765707	0.88[EUR][1000 genomes]
rs766794	0.95[EUR][1000 genomes]
rs7976710	0.88[EUR][1000 genomes]
rs9669050	0.93[EUR][1000 genomes]
rs977069	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049525	chr12:46721742-47264172	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
2	nsv541486	chr12:46721742-47264172	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
3	esv1811918	chr12:46965257-47033254	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv3416674	chr12:46988689-47178369	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv558783	chr12:46996632-47144856	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	esv1814000	chr12:47007493-47033254	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv692	chr12:47018472-47049495	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv1848054	chr12:47018846-47033254	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:47022000-47030800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr12:47023200-47028400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr12:47023200-47032400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr12:47023800-47027200	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr12:47024000-47026800	Weak transcription	Pancreas	Pancrea
6	chr12:47024000-47027200	Weak transcription	Gastric	stomach
7	chr12:47024000-47030800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr12:47025000-47030800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr12:47025200-47026000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr12:47025200-47026000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr12:47025200-47026000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr12:47025200-47026000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr12:47025200-47026000	Enhancers	HSMM	muscle
14	chr12:47025200-47026000	Enhancers	HSMMtube	muscle
15	chr12:47025200-47026000	Enhancers	NHLF	lung
16	chr12:47025200-47026200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr12:47025200-47026200	Enhancers	Muscle Satellite Cultured Cells	--
18	chr12:47025200-47026200	Enhancers	NHDF-Ad	bronchial
19	chr12:47025200-47026200	Enhancers	Osteobl	bone
20	chr12:47025200-47030600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr12:47025400-47026000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr12:47025400-47026000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr12:47025400-47026400	Enhancers	HepG2	liver
24	chr12:47025400-47034000	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr12:47025800-47026000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr12:47025800-47026000	ZNF genes & repeats	Psoas Muscle	Psoas
27	chr12:47025800-47026000	Enhancers	Stomach Mucosa	stomach
28	chr12:47025800-47032200	Weak transcription	NHEK	skin

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