Variant report

Variant	rs3915083
Chromosome Location	chr2:100359701-100359702
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10175788	0.91[ASN][1000 genomes]
rs10182690	0.89[ASN][1000 genomes]
rs10191077	0.80[ASN][1000 genomes]
rs10191816	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10199818	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10204617	0.87[EUR][1000 genomes]
rs10496340	0.87[EUR][1000 genomes]
rs10865032	0.85[EUR][1000 genomes]
rs11123793	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11123794	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11123795	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11123796	0.87[EUR][1000 genomes]
rs11682978	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11690403	0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11888741	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12712059	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13000055	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs13010551	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13030932	0.95[ASN][1000 genomes]
rs13407928	0.95[ASN][1000 genomes]
rs13428668	1.00[ASN][1000 genomes]
rs1404175	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1404176	0.98[ASN][1000 genomes]
rs1404177	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1464757	0.95[ASN][1000 genomes]
rs1568786	0.80[EUR][1000 genomes]
rs2030690	0.86[ASN][1000 genomes]
rs2091150	0.86[ASN][1000 genomes]
rs2115600	0.87[EUR][1000 genomes]
rs2115601	0.89[ASN][1000 genomes]
rs2163044	0.93[ASN][1000 genomes]
rs2309650	0.87[EUR][1000 genomes]
rs2309690	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2309723	0.89[AFR][1000 genomes]
rs2309729	0.81[ASN][1000 genomes]
rs2871316	0.84[ASN][1000 genomes]
rs34116173	0.95[ASN][1000 genomes]
rs34369751	0.95[ASN][1000 genomes]
rs3863005	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3863006	1.00[ASN][1000 genomes]
rs4332968	0.91[ASN][1000 genomes]
rs4850914	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4851225	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4851226	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4851228	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4851229	1.00[ASN][1000 genomes]
rs4851230	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4851231	0.87[EUR][1000 genomes]
rs4851232	0.87[ASN][1000 genomes]
rs4851234	0.87[ASN][1000 genomes]
rs62147565	0.87[EUR][1000 genomes]
rs6542890	1.00[ASN][1000 genomes]
rs6542891	0.88[ASN][1000 genomes]
rs6705966	0.89[ASN][1000 genomes]
rs6708339	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6721652	0.91[ASN][1000 genomes]
rs6732358	0.89[ASN][1000 genomes]
rs6739478	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6739601	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6741990	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6744510	0.95[ASN][1000 genomes]
rs6746146	0.91[ASN][1000 genomes]
rs6748557	0.91[ASN][1000 genomes]
rs6756009	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6756821	0.91[ASN][1000 genomes]
rs6757262	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6758027	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7559975	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7561009	0.82[ASN][1000 genomes]
rs7565155	0.89[ASN][1000 genomes]
rs7573572	0.89[ASN][1000 genomes]
rs7582469	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7584365	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7589376	0.88[ASN][1000 genomes]
rs7602699	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7604536	0.89[ASN][1000 genomes]
rs868665	0.84[ASN][1000 genomes]
rs9308829	0.93[ASN][1000 genomes]
rs940458	0.88[ASN][1000 genomes]
rs9967704	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv431424	chr2:99652682-100494682	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv1003343	chr2:100241560-100848900	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv535843	chr2:100241560-100848900	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:100344000-100360200	Weak transcription	Brain Germinal Matrix	brain
2	chr2:100346200-100379400	Weak transcription	Fetal Lung	lung
3	chr2:100347400-100361600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr2:100356600-100361000	Weak transcription	Fetal Stomach	stomach
5	chr2:100356600-100370400	Weak transcription	Colon Smooth Muscle	Colon
6	chr2:100357600-100369200	Weak transcription	Stomach Smooth Muscle	stomach
7	chr2:100357600-100389400	Weak transcription	Thymus	Thymus
8	chr2:100357800-100361800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr2:100358200-100359800	Weak transcription	Fetal Brain Female	brain
10	chr2:100358200-100370000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr2:100358400-100359800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr2:100358400-100370000	Weak transcription	Spleen	Spleen
13	chr2:100358400-100375400	Strong transcription	Primary B cells from peripheral blood	blood
14	chr2:100358600-100360000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr2:100358600-100360000	Strong transcription	Dnd41	blood
16	chr2:100358600-100360200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr2:100358600-100360400	Strong transcription	Primary T cells from cord blood	blood
18	chr2:100358600-100370000	Weak transcription	NH-A	brain
19	chr2:100358800-100363800	Weak transcription	Left Ventricle	heart
20	chr2:100358800-100375600	Strong transcription	Primary B cells from cord blood	blood
21	chr2:100359000-100359800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr2:100359200-100360400	Strong transcription	Liver	Liver
23	chr2:100359400-100360000	Strong transcription	Ovary	ovary
24	chr2:100359600-100359800	Enhancers	Fetal Brain Male	brain
25	chr2:100359600-100359800	ZNF genes & repeats	Fetal Thymus	thymus
26	chr2:100359600-100379200	Weak transcription	Primary hematopoietic stem cells	blood

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