Variant report

Variant	rs11598344
Chromosome Location	chr10:28248520-28248521
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 95 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs10826357	0.85[ASN][1000 genomes]
rs10826358	0.85[ASN][1000 genomes]
rs10826359	0.86[ASN][1000 genomes]
rs10826360	0.86[ASN][1000 genomes]
rs10826362	0.89[ASN][1000 genomes]
rs10826363	0.92[ASN][1000 genomes]
rs10826364	0.92[ASN][1000 genomes]
rs10826365	0.90[ASN][1000 genomes]
rs10826370	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11006758	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11006759	0.86[ASN][1000 genomes]
rs11006760	0.88[ASN][1000 genomes]
rs11006761	0.88[ASN][1000 genomes]
rs11006762	0.88[ASN][1000 genomes]
rs11006764	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11006765	0.89[ASN][1000 genomes]
rs11006766	0.89[ASN][1000 genomes]
rs11006767	0.89[ASN][1000 genomes]
rs11006769	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11006779	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11006786	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11492473	0.89[ASN][1000 genomes]
rs11595397	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11595783	0.86[ASN][1000 genomes]
rs11596317	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11816757	0.86[ASN][1000 genomes]
rs12358199	0.86[ASN][1000 genomes]
rs12358283	0.86[ASN][1000 genomes]
rs12772278	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12779352	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1334719	0.89[ASN][1000 genomes]
rs1413772	0.88[ASN][1000 genomes]
rs1419366	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1832005	0.89[ASN][1000 genomes]
rs1931889	1.00[ASN][1000 genomes]
rs1970631	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2003192	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2065690	0.88[ASN][1000 genomes]
rs2184418	0.89[ASN][1000 genomes]
rs2297646	1.00[ASN][1000 genomes]
rs2368271	0.89[ASN][1000 genomes]
rs2368272	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2368273	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2368274	0.92[ASN][1000 genomes]
rs3824590	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3952837	0.98[ASN][1000 genomes]
rs4237386	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4265508	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4303140	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4420169	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4494226	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4590766	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4600119	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4628591	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4749274	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4749275	0.88[ASN][1000 genomes]
rs4749276	0.88[ASN][1000 genomes]
rs4749277	0.88[ASN][1000 genomes]
rs4749278	0.89[ASN][1000 genomes]
rs4749279	0.89[ASN][1000 genomes]
rs4749280	0.89[ASN][1000 genomes]
rs4749285	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4749286	0.85[EUR][1000 genomes]
rs4749287	0.86[EUR][1000 genomes]
rs6481490	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6481491	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7070860	0.88[ASN][1000 genomes]
rs7074562	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7077472	0.92[ASN][1000 genomes]
rs7087095	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7089040	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7090390	0.86[ASN][1000 genomes]
rs7094167	0.88[ASN][1000 genomes]
rs7094542	0.89[ASN][1000 genomes]
rs7095239	0.87[ASN][1000 genomes]
rs7095692	0.92[ASN][1000 genomes]
rs7099583	0.86[ASN][1000 genomes]
rs7099871	0.86[ASN][1000 genomes]
rs7099876	0.87[ASN][1000 genomes]
rs7100494	0.86[ASN][1000 genomes]
rs7893462	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7896951	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7897553	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7897889	0.92[ASN][1000 genomes]
rs7907415	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7907500	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7924172	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs880706	0.92[ASN][1000 genomes]
rs880707	0.92[ASN][1000 genomes]
rs880708	0.92[ASN][1000 genomes]
rs9663255	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917149	chr10:28018919-28688694	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv971859	chr10:28070066-28271252	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv894987	chr10:28165502-28326775	ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv831815	chr10:28235661-28407533	Strong transcription Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28224200-28253000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr10:28239800-28287200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr10:28247000-28248600	Enhancers	Dnd41	blood
4	chr10:28248000-28263400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr10:28248200-28248600	Enhancers	Primary T cells fromperipheralblood	blood
6	chr10:28248200-28248600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr10:28248200-28248600	Enhancers	NH-A	brain
8	chr10:28248200-28248800	Enhancers	Osteobl	bone
9	chr10:28248400-28248600	Enhancers	Primary T helper naive cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links