Variant report

Variant	rs4237386
Chromosome Location	chr10:28215740-28215741
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 94 )
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	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11006758	0.90[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	0.92[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	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11006779	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11006786	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11492473	0.89[ASN][1000 genomes]
rs11595397	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11595783	0.86[ASN][1000 genomes]
rs11596317	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11598344	0.93[AMR][1000 genomes];0.96[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	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12779352	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1334719	0.89[ASN][1000 genomes]
rs1413772	0.88[ASN][1000 genomes]
rs1419366	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1832005	0.89[ASN][1000 genomes]
rs1931889	1.00[ASN][1000 genomes]
rs1970631	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2003192	0.85[AMR][1000 genomes];0.93[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	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2368273	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2368274	0.92[ASN][1000 genomes]
rs3824590	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3952837	0.98[ASN][1000 genomes]
rs4265508	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4303140	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4420169	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4494226	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4590766	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4600119	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4628591	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4749274	0.91[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	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4749286	0.86[EUR][1000 genomes]
rs4749287	0.87[EUR][1000 genomes]
rs6481490	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6481491	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7070860	0.88[ASN][1000 genomes]
rs7074562	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7077472	0.92[ASN][1000 genomes]
rs7087095	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7089040	0.91[AMR][1000 genomes];0.97[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];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7896951	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7897553	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7897889	0.92[ASN][1000 genomes]
rs7907415	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7907500	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7924172	0.91[AMR][1000 genomes];0.98[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:3 , 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

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28204000-28223800	Weak transcription	Ovary	ovary
2	chr10:28215200-28221800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links