Variant report

Variant	rs12411068
Chromosome Location	chr1:215288952-215288953
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 112 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:111)

rs_ID	r²[population]
rs10127521	0.98[ASN][1000 genomes]
rs10127656	0.85[CHB][hapmap];0.88[CHD][hapmap];0.81[JPT][hapmap];0.84[ASN][1000 genomes]
rs10746454	0.90[CHB][hapmap]
rs10746455	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10779639	0.90[CHB][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs10779640	0.85[CHB][hapmap];0.81[JPT][hapmap];0.84[ASN][1000 genomes]
rs10779642	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs10779643	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs10779644	0.85[CHB][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs10779645	0.89[CHB][hapmap];0.81[ASN][1000 genomes]
rs10779646	0.95[CHB][hapmap];0.90[JPT][hapmap];0.81[ASN][1000 genomes]
rs10779647	0.85[CHB][hapmap];0.82[CHD][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs10779649	0.95[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10779650	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10779651	0.95[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10779652	0.86[ASN][1000 genomes]
rs10864152	0.81[CHD][hapmap]
rs10864154	0.84[ASN][1000 genomes]
rs10864157	0.83[ASN][1000 genomes]
rs11120495	0.90[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11120496	0.82[ASN][1000 genomes]
rs11120497	0.93[ASN][1000 genomes]
rs11120498	0.82[ASN][1000 genomes]
rs11120499	0.85[CHB][hapmap];0.88[CHD][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs11120500	0.98[ASN][1000 genomes]
rs11120506	0.81[ASN][1000 genomes]
rs11120508	0.85[CHB][hapmap];0.86[CHD][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs11120511	0.89[CHB][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs11120513	0.85[CHB][hapmap];0.86[CHD][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs11120516	0.80[ASN][1000 genomes]
rs1112101	0.95[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs12031308	0.89[CHB][hapmap];0.88[JPT][hapmap];0.81[ASN][1000 genomes]
rs12039875	0.85[CHB][hapmap];0.85[CHD][hapmap]
rs12061916	0.82[ASN][1000 genomes]
rs12062098	0.88[ASN][1000 genomes]
rs12068734	0.81[ASN][1000 genomes]
rs12120091	0.85[CHB][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs12121761	0.85[CHB][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs12135076	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs12138497	0.93[ASN][1000 genomes]
rs12141874	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12143339	0.85[CHB][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs12410041	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12567520	0.95[CHB][hapmap];0.90[CHD][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs12742137	0.84[ASN][1000 genomes]
rs1339405	0.85[CHB][hapmap];0.81[JPT][hapmap]
rs1339406	0.85[CHB][hapmap];0.84[JPT][hapmap]
rs1361340	0.83[CHD][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs1416647	0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1578137	0.90[ASN][1000 genomes]
rs2363554	0.94[CHB][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs2363556	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2363557	0.95[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2363564	0.85[CHB][hapmap];0.85[CHD][hapmap];0.81[JPT][hapmap]
rs2363565	0.85[CHB][hapmap];0.85[CHD][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs2363566	0.95[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2363567	0.95[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2885812	0.83[CHB][hapmap];0.81[ASN][1000 genomes]
rs2885813	0.97[ASN][1000 genomes]
rs2885815	0.85[CHB][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs3931585	0.83[ASN][1000 genomes]
rs4269745	0.97[ASN][1000 genomes]
rs4271184	0.81[CHB][hapmap];0.83[CHD][hapmap]
rs4300189	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4303048	0.95[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs4375232	0.83[CHB][hapmap]
rs4411107	0.85[CHB][hapmap];0.88[CHD][hapmap];0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs4428856	0.82[ASN][1000 genomes]
rs4497183	0.85[CHB][hapmap];0.88[CHD][hapmap];0.85[JPT][hapmap];0.81[ASN][1000 genomes]
rs4509552	0.81[ASN][1000 genomes]
rs4509553	0.85[CHB][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs4531266	0.89[CHB][hapmap];0.84[ASN][1000 genomes]
rs4548407	0.85[ASN][1000 genomes]
rs4556330	0.81[CHB][hapmap]
rs4571941	0.81[ASN][1000 genomes]
rs4573492	0.82[ASN][1000 genomes]
rs4607848	0.98[ASN][1000 genomes]
rs4655276	0.81[ASN][1000 genomes]
rs4655277	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs4655278	0.95[ASN][1000 genomes]
rs4655391	0.85[CHB][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs4655392	0.90[CHB][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs4655393	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs4655394	0.95[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs4655395	0.94[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs61818320	0.98[ASN][1000 genomes]
rs61818328	0.97[ASN][1000 genomes]
rs6657313	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6662353	0.95[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6666828	0.85[CHB][hapmap];0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs6667764	0.85[CHB][hapmap];0.81[JPT][hapmap]
rs6672978	0.85[CHB][hapmap];0.86[CHD][hapmap];0.81[JPT][hapmap]
rs6673739	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6675926	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs6678758	0.97[ASN][1000 genomes]
rs6683041	0.82[ASN][1000 genomes]
rs6684084	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs6695343	0.86[ASN][1000 genomes]
rs6695967	0.97[ASN][1000 genomes]
rs6696333	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6699161	0.90[CHB][hapmap];0.88[CHD][hapmap]
rs72735359	0.97[ASN][1000 genomes]
rs7417100	0.85[CHB][hapmap];0.81[ASN][1000 genomes]
rs7513709	0.85[CHB][hapmap];0.81[JPT][hapmap];0.84[ASN][1000 genomes]
rs7540029	0.85[ASN][1000 genomes]
rs7541543	0.85[CHB][hapmap];0.88[CHD][hapmap];0.81[JPT][hapmap];0.84[ASN][1000 genomes]
rs7547572	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7547655	0.81[CHB][hapmap]
rs7549136	0.85[CHB][hapmap];0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs9793382	0.85[ASN][1000 genomes]
rs9793690	0.88[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873169	chr1:215264486-215453286	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215283400-215291200	Weak transcription	Fetal Brain Female	brain
2	chr1:215286600-215289000	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr1:215286600-215289000	Enhancers	NHEK	skin
4	chr1:215286800-215289000	Enhancers	HMEC	breast
5	chr1:215287000-215293800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr1:215287200-215289400	Enhancers	Hela-S3	cervix
7	chr1:215287800-215289000	Enhancers	NHDF-Ad	bronchial
8	chr1:215287800-215289000	Enhancers	Osteobl	bone
9	chr1:215287800-215290200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr1:215288200-215290000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:215288200-215294000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:215288400-215289600	Enhancers	HUVEC	blood vessel
13	chr1:215288600-215290400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:215288800-215289000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr1:215288800-215289000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr1:215288800-215306600	Weak transcription	NHLF	lung

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