Variant report

Variant	rs2780213
Chromosome Location	chr9:17406381-17406382
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 174 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:151)

rs_ID	r²[population]
rs10115784	1.00[CEU][hapmap]
rs10117379	0.95[ASN][1000 genomes]
rs10119233	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10119863	0.95[ASN][1000 genomes]
rs10119902	0.95[ASN][1000 genomes]
rs10120006	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10120013	0.95[ASN][1000 genomes]
rs10120733	1.00[CHB][hapmap];0.95[CHD][hapmap];0.93[JPT][hapmap];0.83[MEX][hapmap];0.92[ASN][1000 genomes]
rs10120761	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10125886	0.95[ASN][1000 genomes]
rs1023778	0.94[CHB][hapmap];0.87[JPT][hapmap];0.89[ASN][1000 genomes]
rs10738477	0.95[ASN][1000 genomes]
rs10756879	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10810764	0.82[JPT][hapmap]
rs10810783	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10962922	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs10962924	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs10962939	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs10962995	1.00[CEU][hapmap]
rs10963056	1.00[CEU][hapmap]
rs10963067	1.00[CEU][hapmap]
rs10963070	1.00[CEU][hapmap]
rs10963081	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10963085	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10963088	0.99[ASN][1000 genomes]
rs10963103	0.91[CEU][hapmap];0.86[CHB][hapmap];0.92[JPT][hapmap];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10963105	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1113379	0.88[CHB][hapmap];0.80[CHD][hapmap];0.80[JPT][hapmap]
rs1113380	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs12235811	0.92[CEU][hapmap]
rs1318162	0.87[JPT][hapmap]
rs1372700	0.97[ASN][1000 genomes]
rs1372704	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1413418	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs1413419	0.80[JPT][hapmap]
rs1442518	0.95[ASN][1000 genomes]
rs1442520	0.95[ASN][1000 genomes]
rs1442521	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1442522	0.85[ASW][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.95[ASN][1000 genomes]
rs1442525	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1442526	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.96[ASN][1000 genomes]
rs1442527	0.85[LWK][hapmap]
rs1576958	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs1582029	0.88[CHB][hapmap];0.80[CHD][hapmap];0.80[JPT][hapmap]
rs1583985	1.00[CEU][hapmap]
rs16935416	1.00[CEU][hapmap]
rs1759452	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs1759453	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs1759458	0.81[CHB][hapmap];0.80[CHD][hapmap];0.80[JPT][hapmap]
rs1759459	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs1759460	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs1759462	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs1759463	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs1759465	0.81[CHB][hapmap];0.80[CHD][hapmap]
rs1759616	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs1930639	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs1930641	0.81[CHB][hapmap];0.80[CHD][hapmap];0.80[JPT][hapmap]
rs1930647	0.91[ASN][1000 genomes]
rs1930648	0.95[ASN][1000 genomes]
rs2010086	0.85[ASN][1000 genomes]
rs2039413	0.88[CHB][hapmap]
rs2083694	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2119906	0.95[ASN][1000 genomes]
rs2119907	0.89[ASN][1000 genomes]
rs2165688	0.82[ASN][1000 genomes]
rs2274916	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.86[TSI][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2441991	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2584539	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2584546	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2584548	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2584549	0.99[ASN][1000 genomes]
rs2584550	0.95[ASN][1000 genomes]
rs2584551	0.97[ASN][1000 genomes]
rs2584552	0.84[EUR][1000 genomes]
rs2593388	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2593389	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];1.00[ASN][1000 genomes]
rs2593390	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2593397	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2593416	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2593418	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2780203	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2780204	0.81[CHB][hapmap];0.80[CHD][hapmap];0.80[JPT][hapmap]
rs2780205	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs2780208	0.95[ASN][1000 genomes]
rs2780210	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2780211	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2780214	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.97[ASN][1000 genomes]
rs3739488	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.96[ASN][1000 genomes]
rs3739489	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.86[TSI][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3808781	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs3808782	1.00[CEU][hapmap]
rs3808785	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs3814137	0.88[CHB][hapmap];0.80[CHD][hapmap];0.80[JPT][hapmap]
rs3814139	0.88[CHB][hapmap];0.80[CHD][hapmap];0.80[JPT][hapmap]
rs3891457	0.93[CHB][hapmap];0.81[YRI][hapmap]
rs4147023	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs4554574	1.00[CEU][hapmap]
rs4621917	0.94[CHB][hapmap];0.91[CHD][hapmap];0.80[JPT][hapmap]
rs4961534	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs4961551	0.94[CHB][hapmap];0.91[CHD][hapmap];0.82[JPT][hapmap];0.83[MEX][hapmap];0.82[ASN][1000 genomes]
rs4961554	0.94[CHB][hapmap];0.91[CHD][hapmap];0.80[JPT][hapmap];0.86[ASN][1000 genomes]
rs4961556	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs5001765	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs600041	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs600133	0.81[CHB][hapmap];0.80[CHD][hapmap];0.80[JPT][hapmap]
rs601960	0.81[CHB][hapmap];0.80[CHD][hapmap]
rs613966	0.81[CHB][hapmap];0.80[CHD][hapmap];0.80[JPT][hapmap]
rs614412	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs614471	0.81[CHB][hapmap];0.80[CHD][hapmap];0.80[JPT][hapmap]
rs620280	0.91[CEU][hapmap]
rs632176	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs634383	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs634446	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs642582	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs646025	0.81[CHB][hapmap];0.80[CHD][hapmap];0.80[JPT][hapmap];0.81[MEX][hapmap]
rs647013	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs6475122	0.88[CHB][hapmap];0.80[CHD][hapmap];0.80[JPT][hapmap]
rs6475123	1.00[CEU][hapmap]
rs6475125	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs6475129	0.81[CHB][hapmap];0.80[CHD][hapmap];0.80[JPT][hapmap]
rs6475140	1.00[CEU][hapmap]
rs664447	0.88[CHB][hapmap];0.80[CHD][hapmap];0.80[JPT][hapmap]
rs673587	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs679666	0.81[CHB][hapmap];0.80[CHD][hapmap]
rs7020918	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs7023305	0.95[ASN][1000 genomes]
rs7023540	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7026207	0.88[LWK][hapmap]
rs7027292	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.95[ASN][1000 genomes]
rs7027539	0.94[CHB][hapmap];0.91[CHD][hapmap];0.80[JPT][hapmap];0.83[MEX][hapmap];0.86[ASN][1000 genomes]
rs7031133	0.81[JPT][hapmap]
rs7031361	1.00[CEU][hapmap]
rs7034768	0.88[CHB][hapmap];0.80[CHD][hapmap];0.80[JPT][hapmap]
rs7035276	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.96[ASN][1000 genomes]
rs7035357	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.95[ASN][1000 genomes]
rs7035525	0.88[CHB][hapmap]
rs7037041	0.82[ASN][1000 genomes]
rs7042700	0.94[CHB][hapmap];0.83[ASN][1000 genomes]
rs7043703	0.88[CHB][hapmap];0.80[CHD][hapmap]
rs7046327	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs7047093	0.88[CHB][hapmap];0.80[JPT][hapmap];0.86[ASN][1000 genomes]
rs7865807	0.94[CHB][hapmap];0.80[JPT][hapmap]
rs7870334	1.00[CEU][hapmap];0.87[CHB][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];0.87[JPT][hapmap];0.93[MEX][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7870427	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7872910	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7873708	0.82[JPT][hapmap]
rs7874945	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.96[ASN][1000 genomes]
rs870270	0.88[CHB][hapmap];0.80[CHD][hapmap];0.80[JPT][hapmap]
rs9298777	0.95[ASN][1000 genomes]
rs9298778	0.93[ASN][1000 genomes]
rs9657595	0.92[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024799	chr9:16631890-17431827	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv892658	chr9:17041557-17532840	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	nsv892661	chr9:17134245-17532840	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv613693	chr9:17147191-17710407	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
5	nsv471287	chr9:17165698-17708814	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv466269	chr9:17165698-17710407	Weak transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
7	nsv466271	chr9:17329964-17438391	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv613696	chr9:17329964-17438391	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1015524	chr9:17350843-17419424	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv892668	chr9:17371690-17532840	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
11	nsv892669	chr9:17378776-17438391	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv892670	chr9:17378776-17507277	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
13	nsv892671	chr9:17378776-17610211	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
14	nsv466273	chr9:17391531-17436662	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv613697	chr9:17391531-17436662	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv523411	chr9:17394536-17454799	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
17	esv2422265	chr9:17396711-17598187	Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
18	esv19349	chr9:17401160-17406972	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv3482044	chr9:17401291-17407141	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
20	esv3482046	chr9:17401322-17407173	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
21	esv3482045	chr9:17401350-17407090	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
22	esv3482043	chr9:17401449-17406988	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
23	esv3482047	chr9:17401449-17406988	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17368400-17457800	Weak transcription	Pancreas	Pancrea
2	chr9:17368600-17411200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr9:17368600-17411400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr9:17368600-17411400	Weak transcription	Aorta	Aorta
5	chr9:17368800-17411400	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr9:17369400-17411200	Weak transcription	Fetal Muscle Trunk	muscle
7	chr9:17380600-17411000	Weak transcription	Left Ventricle	heart
8	chr9:17381000-17411200	Weak transcription	Fetal Muscle Leg	muscle
9	chr9:17381200-17411200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr9:17381400-17422800	Weak transcription	Colon Smooth Muscle	Colon
11	chr9:17385400-17411400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr9:17387000-17411200	Weak transcription	Dnd41	blood
13	chr9:17388200-17411400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr9:17391600-17411200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr9:17393400-17411400	Weak transcription	Lung	lung
16	chr9:17393400-17433000	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr9:17393600-17412800	Weak transcription	Fetal Kidney	kidney
18	chr9:17393600-17413000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr9:17393800-17413000	Weak transcription	A549	lung
20	chr9:17395400-17413600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr9:17395400-17417800	Weak transcription	NHDF-Ad	bronchial
22	chr9:17395600-17410600	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr9:17395600-17411200	Weak transcription	Fetal Lung	lung
24	chr9:17396000-17410800	Weak transcription	Primary hematopoietic stem cells	blood
25	chr9:17396200-17413200	Weak transcription	Stomach Smooth Muscle	stomach
26	chr9:17396200-17440000	Weak transcription	Adipose Nuclei	Adipose
27	chr9:17396800-17411000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr9:17397400-17411000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr9:17397800-17411000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr9:17397800-17411200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr9:17398800-17430600	Weak transcription	HSMM	muscle
32	chr9:17399000-17407600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr9:17399000-17411200	Weak transcription	Ovary	ovary
34	chr9:17399200-17411000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr9:17399200-17411200	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr9:17399400-17425400	Weak transcription	Fetal Heart	heart
37	chr9:17400400-17407000	Weak transcription	Liver	Liver
38	chr9:17405200-17411200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr9:17406000-17411200	Weak transcription	Fetal Stomach	stomach
40	chr9:17406200-17411000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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