Variant report

Variant	rs11183536
Chromosome Location	chr12:46995368-46995369
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 153 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:148)

rs_ID	r²[population]
rs10785631	1.00[CEU][hapmap];0.84[AMR][1000 genomes]
rs10880975	1.00[CEU][hapmap];0.84[AMR][1000 genomes]
rs10880976	1.00[CEU][hapmap];0.84[AMR][1000 genomes]
rs10880977	1.00[CEU][hapmap];0.87[AMR][1000 genomes]
rs10880980	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11183497	1.00[CEU][hapmap]
rs11183507	0.84[AMR][1000 genomes]
rs11183524	1.00[EUR][1000 genomes]
rs11183539	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11183547	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11183550	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11829502	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs11830099	0.95[EUR][1000 genomes]
rs11830501	0.95[EUR][1000 genomes]
rs11831177	1.00[CEU][hapmap]
rs11831920	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs11831929	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs11832316	0.95[EUR][1000 genomes]
rs11833393	1.00[EUR][1000 genomes]
rs11834607	1.00[EUR][1000 genomes]
rs11835517	0.95[EUR][1000 genomes]
rs11835974	0.95[EUR][1000 genomes]
rs11836915	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs11836940	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs11837104	0.95[EUR][1000 genomes]
rs12300125	1.00[CEU][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12305921	1.00[CEU][hapmap]
rs12310635	0.84[EUR][1000 genomes]
rs12578813	0.88[EUR][1000 genomes]
rs12579089	0.88[EUR][1000 genomes]
rs12579348	0.95[EUR][1000 genomes]
rs12579976	0.95[EUR][1000 genomes]
rs12580092	0.95[EUR][1000 genomes]
rs12580121	1.00[CEU][hapmap]
rs12580356	0.88[EUR][1000 genomes]
rs12580488	0.85[EUR][1000 genomes]
rs12581311	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12581366	0.88[EUR][1000 genomes]
rs12582013	0.85[EUR][1000 genomes]
rs12582056	1.00[CEU][hapmap];0.94[JPT][hapmap];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12582305	1.00[CEU][hapmap]
rs12582476	0.88[EUR][1000 genomes]
rs17096991	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17096995	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs17097002	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs17097009	0.95[EUR][1000 genomes]
rs17097022	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs17121410	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17121412	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs17594275	0.85[EUR][1000 genomes]
rs17611638	0.88[EUR][1000 genomes]
rs1946175	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2042058	1.00[CEU][hapmap];0.94[JPT][hapmap];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2193662	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2193663	0.95[EUR][1000 genomes]
rs2216439	0.91[EUR][1000 genomes]
rs235601	0.93[EUR][1000 genomes]
rs235602	0.93[EUR][1000 genomes]
rs235607	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs235610	0.93[EUR][1000 genomes]
rs235616	0.86[EUR][1000 genomes]
rs235617	1.00[CEU][hapmap]
rs235621	1.00[CEU][hapmap];0.94[JPT][hapmap];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs235622	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs235625	0.90[EUR][1000 genomes]
rs235626	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs235627	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2408576	0.95[EUR][1000 genomes]
rs2408577	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2430937	1.00[EUR][1000 genomes]
rs2430939	1.00[EUR][1000 genomes]
rs2430940	1.00[CEU][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2430941	1.00[EUR][1000 genomes]
rs2430942	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2430943	1.00[EUR][1000 genomes]
rs2430946	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs2430947	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs2471581	0.88[EUR][1000 genomes]
rs2471583	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2471588	1.00[EUR][1000 genomes]
rs2471594	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2471601	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2471602	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2471605	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2471608	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2471617	1.00[EUR][1000 genomes]
rs2471618	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs28768973	1.00[EUR][1000 genomes]
rs2897969	0.91[EUR][1000 genomes]
rs2909411	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2960450	1.00[EUR][1000 genomes]
rs34008890	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35096979	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4073924	0.88[EUR][1000 genomes]
rs4604970	0.95[EUR][1000 genomes]
rs4768125	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4768731	0.87[AMR][1000 genomes]
rs4768741	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs4768742	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4768744	1.00[CEU][hapmap];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56111534	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs56152575	0.95[EUR][1000 genomes]
rs56181923	0.95[EUR][1000 genomes]
rs56271434	0.95[EUR][1000 genomes]
rs56399247	0.88[EUR][1000 genomes]
rs57158113	0.88[EUR][1000 genomes]
rs57370043	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs57439008	0.87[AMR][1000 genomes]
rs57658610	1.00[EUR][1000 genomes]
rs58449317	0.95[EUR][1000 genomes]
rs58503088	0.95[EUR][1000 genomes]
rs58561072	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs58813899	0.95[EUR][1000 genomes]
rs59521025	0.87[AMR][1000 genomes]
rs59903937	0.95[EUR][1000 genomes]
rs60191997	1.00[EUR][1000 genomes]
rs60432604	0.88[EUR][1000 genomes]
rs60669661	0.95[EUR][1000 genomes]
rs60681792	0.95[EUR][1000 genomes]
rs61072098	0.97[EUR][1000 genomes]
rs61355826	1.00[EUR][1000 genomes]
rs61641663	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6582666	1.00[CEU][hapmap];0.87[AMR][1000 genomes]
rs7138914	0.95[EUR][1000 genomes]
rs7295471	1.00[CEU][hapmap];0.87[AMR][1000 genomes]
rs7302876	0.86[EUR][1000 genomes]
rs7308386	0.95[EUR][1000 genomes]
rs7310326	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7310408	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73282109	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73290381	0.88[EUR][1000 genomes]
rs73290402	0.95[EUR][1000 genomes]
rs73291964	0.95[EUR][1000 genomes]
rs73291976	0.95[EUR][1000 genomes]
rs73291980	0.95[EUR][1000 genomes]
rs73292000	0.95[EUR][1000 genomes]
rs73292001	1.00[EUR][1000 genomes]
rs73293911	0.95[EUR][1000 genomes]
rs73293919	0.95[EUR][1000 genomes]
rs7484802	0.83[EUR][1000 genomes]
rs7488464	1.00[EUR][1000 genomes]
rs765707	0.95[EUR][1000 genomes]
rs766794	0.88[EUR][1000 genomes]
rs7976710	0.95[EUR][1000 genomes]
rs9669050	1.00[EUR][1000 genomes]
rs977069	1.00[CEU][hapmap];0.94[JPT][hapmap];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9783500	0.87[AMR][1000 genomes]
rs9971651	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1842882	chr12:46691487-47009428	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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
5	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

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:46980200-46995600	Weak transcription	Gastric	stomach
2	chr12:46980200-47002000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr12:46980200-47002200	Weak transcription	Thymus	Thymus
4	chr12:46980200-47002800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr12:46985200-46997400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr12:46985200-47002200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr12:46985400-47002200	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr12:46985600-47007000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr12:46991400-47000600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr12:46994200-46998000	Enhancers	Dnd41	blood
11	chr12:46994600-46995400	Enhancers	Psoas Muscle	Psoas
12	chr12:46994800-47002200	Weak transcription	NHEK	skin
13	chr12:46995000-46996000	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
14	chr12:46995200-46995800	Enhancers	H1 Cell Line	embryonic stem cell
15	chr12:46995200-46995800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr12:46995200-46995800	Enhancers	Fetal Thymus	thymus

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