Variant report

Variant	rs305396
Chromosome Location	chr12:73022080-73022081
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 98 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs10735970	0.82[ASN][1000 genomes]
rs10748202	0.86[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs10748203	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs10784975	0.86[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs10784978	0.88[ASN][1000 genomes]
rs10784979	0.80[ASN][1000 genomes]
rs10879461	0.88[ASN][1000 genomes]
rs10879462	0.88[ASN][1000 genomes]
rs10879464	0.93[ASN][1000 genomes]
rs10879465	0.94[ASN][1000 genomes]
rs10879466	0.94[ASN][1000 genomes]
rs10879472	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10879473	0.85[ASN][1000 genomes]
rs11179280	0.86[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs11179289	0.87[CHB][hapmap];0.85[ASN][1000 genomes]
rs11179290	0.81[CHB][hapmap];0.85[ASN][1000 genomes]
rs11179293	0.83[CHB][hapmap];0.82[ASN][1000 genomes]
rs11179298	0.83[CHB][hapmap];0.87[CHD][hapmap];0.85[ASN][1000 genomes]
rs11179302	0.87[CHB][hapmap];0.85[ASN][1000 genomes]
rs11179307	0.87[CHB][hapmap];0.85[ASN][1000 genomes]
rs11179308	0.90[CHB][hapmap];0.85[ASN][1000 genomes]
rs11179309	0.82[ASN][1000 genomes]
rs11610020	0.85[ASN][1000 genomes]
rs11613768	0.87[CHB][hapmap];0.91[CHD][hapmap];0.85[ASN][1000 genomes]
rs12099552	0.87[CHB][hapmap];0.91[CHD][hapmap];0.85[ASN][1000 genomes]
rs1214894	0.82[CHB][hapmap]
rs1214897	0.82[CHB][hapmap]
rs1214899	0.82[CHB][hapmap];0.82[MEX][hapmap];0.81[TSI][hapmap]
rs12581283	0.82[JPT][hapmap]
rs12582138	0.83[CHB][hapmap];0.85[ASN][1000 genomes]
rs12821081	0.81[CHB][hapmap]
rs1347194	0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs1347196	0.88[ASN][1000 genomes]
rs1389497	0.82[CHB][hapmap]
rs1469721	0.85[ASN][1000 genomes]
rs1560742	0.87[CHB][hapmap];0.91[CHD][hapmap];0.85[ASN][1000 genomes]
rs1560743	0.85[ASN][1000 genomes]
rs1817885	0.82[CHB][hapmap]
rs1836042	0.88[ASN][1000 genomes]
rs1836043	0.88[ASN][1000 genomes]
rs1836044	0.88[ASN][1000 genomes]
rs1864837	0.89[ASN][1000 genomes]
rs1864838	0.86[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs1965318	0.81[CHB][hapmap];0.95[JPT][hapmap]
rs1991751	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2130660	0.81[CHB][hapmap]
rs2887071	0.82[CHB][hapmap]
rs305402	0.81[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs305403	0.88[ASN][1000 genomes]
rs34115559	0.85[ASN][1000 genomes]
rs34893785	0.85[ASN][1000 genomes]
rs35902343	0.83[CHB][hapmap];0.87[CHD][hapmap];0.85[ASN][1000 genomes]
rs3782367	0.82[CHB][hapmap]
rs3843025	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs3852549	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs3852550	0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs3910234	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs3936356	0.83[CHB][hapmap];0.89[CHD][hapmap];0.84[ASN][1000 genomes]
rs3952786	0.87[CHB][hapmap];0.81[ASN][1000 genomes]
rs4100196	0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs41387445	0.81[CHD][hapmap]
rs458942	0.97[ASN][1000 genomes]
rs460406	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.92[MKK][hapmap];0.88[TSI][hapmap];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6582094	0.88[ASN][1000 genomes]
rs6582095	0.87[ASN][1000 genomes]
rs66495167	0.85[ASN][1000 genomes]
rs683101	0.82[CHB][hapmap]
rs7131984	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs7135547	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs71457035	0.91[ASN][1000 genomes]
rs723867	0.82[CHB][hapmap]
rs7297703	0.87[CHB][hapmap];0.86[CHD][hapmap];0.85[ASN][1000 genomes]
rs7299196	0.87[CHB][hapmap];0.85[ASN][1000 genomes]
rs7299984	0.90[ASN][1000 genomes]
rs7303841	0.87[CHB][hapmap];0.89[CHD][hapmap];0.85[ASN][1000 genomes]
rs7309263	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs7309330	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7309651	0.91[ASN][1000 genomes]
rs7967001	0.82[CHB][hapmap];0.83[CHD][hapmap];0.95[JPT][hapmap]
rs7969680	0.89[ASN][1000 genomes]
rs7969934	0.88[ASN][1000 genomes]
rs9705508	0.83[ASN][1000 genomes]
rs972421	0.87[CHB][hapmap];0.89[CHD][hapmap];0.85[ASN][1000 genomes]
rs996575	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422452	chr12:72485933-73175581	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv899257	chr12:72569746-73145896	ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	nsv1044083	chr12:72647640-73275526	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv469465	chr12:72655925-73259114	Weak transcription Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv559363	chr12:72655925-73259114	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv868884	chr12:72664763-73241518	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv817280	chr12:72820558-73508605	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
8	nsv832454	chr12:72940798-73081180	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1054725	chr12:72990553-73062598	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	esv2758314	chr12:72990707-73251109	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	esv2759908	chr12:72990707-73251109	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv868885	chr12:72998553-73587081	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
13	nsv1048951	chr12:73018354-73151893	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv1052520	chr12:73018354-73181472	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:73005000-73051600	Weak transcription	Fetal Intestine Large	intestine
2	chr12:73005200-73038000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr12:73005200-73053200	Weak transcription	Ovary	ovary
4	chr12:73011400-73059000	Weak transcription	Pancreas	Pancrea
5	chr12:73014400-73042000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr12:73014800-73055800	Weak transcription	Adipose Nuclei	Adipose
7	chr12:73020400-73022800	Weak transcription	NH-A	brain

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