Variant report

Variant	rs10863030
Chromosome Location	chr12:86034033-86034034
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 130 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:114)

rs_ID	r²[population]
rs10863013	0.90[ASN][1000 genomes]
rs10863014	0.90[ASN][1000 genomes]
rs10863024	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10863025	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10863042	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10863051	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11116852	1.00[CEU][hapmap]
rs11116861	0.90[ASN][1000 genomes]
rs11116866	0.90[ASN][1000 genomes]
rs11116867	0.90[ASN][1000 genomes]
rs11116868	0.90[ASN][1000 genomes]
rs11116869	0.90[ASN][1000 genomes]
rs11116870	0.90[ASN][1000 genomes]
rs11116874	0.90[ASN][1000 genomes]
rs11116875	0.90[ASN][1000 genomes]
rs11116876	0.90[ASN][1000 genomes]
rs11116880	0.90[ASN][1000 genomes]
rs11116881	0.90[ASN][1000 genomes]
rs11116882	0.90[ASN][1000 genomes]
rs11116884	0.90[ASN][1000 genomes]
rs11116885	0.90[ASN][1000 genomes]
rs11116887	0.90[ASN][1000 genomes]
rs11116889	0.90[ASN][1000 genomes]
rs11116890	0.90[ASN][1000 genomes]
rs11116892	0.90[ASN][1000 genomes]
rs11116895	0.90[ASN][1000 genomes]
rs11116896	0.90[ASN][1000 genomes]
rs11116898	0.90[ASN][1000 genomes]
rs11116899	0.90[ASN][1000 genomes]
rs11116920	0.90[ASN][1000 genomes]
rs11116932	0.93[ASN][1000 genomes]
rs11116936	0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11116938	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11116944	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11116950	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11116970	0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11116973	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11116977	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11513953	0.90[ASN][1000 genomes]
rs11832292	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11833053	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11835255	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12227817	0.90[ASN][1000 genomes]
rs12228112	0.90[ASN][1000 genomes]
rs12228412	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12228703	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12231153	0.90[ASN][1000 genomes]
rs12231156	0.90[ASN][1000 genomes]
rs12231815	0.90[ASN][1000 genomes]
rs12231930	0.90[ASN][1000 genomes]
rs12308539	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12308540	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12308608	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12316799	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12316860	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1564123	0.99[ASN][1000 genomes]
rs17013154	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2405253	0.94[ASN][1000 genomes]
rs34506479	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3884595	0.90[ASN][1000 genomes]
rs4143507	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4409917	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4554972	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55827526	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55897445	0.90[ASN][1000 genomes]
rs57527697	0.90[ASN][1000 genomes]
rs57608040	0.90[ASN][1000 genomes]
rs57741929	0.90[ASN][1000 genomes]
rs58809157	0.90[ASN][1000 genomes]
rs59312748	0.90[ASN][1000 genomes]
rs59403304	0.90[ASN][1000 genomes]
rs59788521	0.90[ASN][1000 genomes]
rs60202749	0.90[ASN][1000 genomes]
rs60683378	0.90[ASN][1000 genomes]
rs6539908	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6539909	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7131964	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7137284	0.90[ASN][1000 genomes]
rs7304792	0.90[ASN][1000 genomes]
rs7313388	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73367235	0.90[ASN][1000 genomes]
rs73367237	0.90[ASN][1000 genomes]
rs73367241	0.90[ASN][1000 genomes]
rs73367246	0.90[ASN][1000 genomes]
rs73367251	0.90[ASN][1000 genomes]
rs73367261	0.90[ASN][1000 genomes]
rs73367266	0.90[ASN][1000 genomes]
rs73367273	0.90[ASN][1000 genomes]
rs73368476	0.90[ASN][1000 genomes]
rs73368490	0.90[ASN][1000 genomes]
rs73368493	0.90[ASN][1000 genomes]
rs73370465	0.89[ASN][1000 genomes]
rs74112222	0.90[ASN][1000 genomes]
rs74112251	0.90[ASN][1000 genomes]
rs74112259	0.90[ASN][1000 genomes]
rs74112289	0.90[ASN][1000 genomes]
rs74112507	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7484736	0.90[ASN][1000 genomes]
rs7485150	0.90[ASN][1000 genomes]
rs7485219	0.89[ASN][1000 genomes]
rs7486870	0.90[ASN][1000 genomes]
rs7486887	0.85[CEU][hapmap];0.86[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7486989	0.90[ASN][1000 genomes]
rs7489034	0.90[ASN][1000 genomes]
rs7966898	0.81[YRI][hapmap]
rs7972133	0.90[ASN][1000 genomes]
rs7977072	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs922340	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9943733	0.90[ASN][1000 genomes]
rs9943736	0.89[ASN][1000 genomes]
rs9943770	0.90[ASN][1000 genomes]
rs9943779	0.90[ASN][1000 genomes]
rs9989016	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9989038	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817242	chr12:85622245-86069213	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1054573	chr12:85658602-86235433	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1035600	chr12:85661373-86235433	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	esv2751125	chr12:85884858-86098240	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1043253	chr12:85888151-86125364	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1037938	chr12:85902517-86045125	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	esv2761758	chr12:85906092-86045137	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv559665	chr12:85908396-86070692	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	esv2751126	chr12:85912432-86061403	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv1052187	chr12:85954455-86278200	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	nsv541560	chr12:85954455-86278200	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
12	nsv1054475	chr12:85985510-86175711	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv541561	chr12:85985510-86175711	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv430522	chr12:86010755-86069542	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
15	nsv1042467	chr12:86017619-86078149	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
16	nsv522439	chr12:86020998-86066266	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86032600-86037000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr12:86033400-86034200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr12:86033800-86035400	Weak transcription	Osteobl	bone

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