Variant report

Variant	rs10895119
Chromosome Location	chr11:101366191-101366192
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 113 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:108)

rs_ID	r²[population]
rs10160542	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10160655	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10501979	1.00[CHB][hapmap]
rs10501980	0.82[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10501981	0.82[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10501986	0.82[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10750606	0.91[JPT][hapmap];0.81[YRI][hapmap]
rs10791477	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10791478	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10791479	0.82[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10791480	0.86[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10791481	1.00[JPT][hapmap];0.87[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10791482	0.87[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10791483	0.86[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10791485	0.82[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10791486	1.00[JPT][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10791487	0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs10791488	0.94[ASN][1000 genomes]
rs10791489	0.94[ASN][1000 genomes]
rs10791490	0.82[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10791491	0.94[ASN][1000 genomes]
rs10895116	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10895117	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs10895118	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10895121	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10895122	1.00[CHB][hapmap]
rs10895123	1.00[JPT][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10895124	0.82[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.87[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10895125	0.82[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs10895126	0.85[JPT][hapmap]
rs10895127	0.84[JPT][hapmap]
rs10895128	0.83[JPT][hapmap]
rs11224784	0.96[YRI][hapmap];0.85[AFR][1000 genomes]
rs11224785	0.80[CEU][hapmap];0.96[YRI][hapmap];0.87[AFR][1000 genomes]
rs11224787	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11224789	0.86[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs11224790	1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs11224791	0.82[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs11224792	0.82[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs11224800	0.82[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs11224801	0.82[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs11224802	0.82[CHB][hapmap]
rs11224806	0.82[CHB][hapmap]
rs11821584	0.81[CEU][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes]
rs11826165	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs12222976	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs12270234	0.81[CEU][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs12361641	0.96[YRI][hapmap];0.86[AFR][1000 genomes]
rs12787386	0.81[CEU][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes]
rs12789670	0.81[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes]
rs12796163	0.94[AFR][1000 genomes]
rs17674687	0.82[CHB][hapmap]
rs17742220	0.82[CHB][hapmap]
rs34546081	0.88[AFR][1000 genomes]
rs4129253	1.00[CHB][hapmap]
rs4129254	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4129255	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4262694	0.82[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs4272759	0.82[CHB][hapmap]
rs4275596	0.85[JPT][hapmap]
rs4403777	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4477408	0.82[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs4533005	0.94[ASN][1000 genomes]
rs4542378	0.82[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs4578354	0.94[ASN][1000 genomes]
rs61915999	0.94[AFR][1000 genomes]
rs6590866	0.81[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes]
rs6590867	0.80[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs6590868	0.88[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs6590869	0.82[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs6590870	0.82[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs6590872	1.00[JPT][hapmap];0.92[YRI][hapmap];0.91[ASN][1000 genomes]
rs6590873	0.91[ASN][1000 genomes]
rs6590874	0.82[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.91[ASN][1000 genomes]
rs6590875	0.82[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs6590876	0.86[ASN][1000 genomes]
rs6590877	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs68106103	0.93[ASN][1000 genomes]
rs7104033	0.94[ASN][1000 genomes]
rs7105161	0.94[ASN][1000 genomes]
rs7115999	0.92[JPT][hapmap]
rs7116473	0.85[JPT][hapmap]
rs7123199	0.89[YRI][hapmap]
rs7127243	0.84[JPT][hapmap];0.85[YRI][hapmap]
rs7924434	0.81[CEU][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes]
rs7924551	1.00[YRI][hapmap];0.93[AFR][1000 genomes]
rs7925012	0.84[JPT][hapmap]
rs7927661	0.82[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7927664	0.81[CEU][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs7927674	0.93[ASN][1000 genomes]
rs7927797	0.91[ASN][1000 genomes]
rs7927803	0.91[ASN][1000 genomes]
rs7927852	0.85[JPT][hapmap]
rs7927859	0.84[JPT][hapmap]
rs7930876	0.87[ASN][1000 genomes]
rs7931830	1.00[YRI][hapmap];0.93[AFR][1000 genomes]
rs7932073	0.81[CEU][hapmap];0.96[YRI][hapmap]
rs7932871	0.82[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7933359	0.94[ASN][1000 genomes]
rs7934021	0.96[YRI][hapmap];0.88[AFR][1000 genomes]
rs7934116	0.92[JPT][hapmap];0.81[YRI][hapmap]
rs7934208	0.82[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7934219	1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7935702	0.82[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7937745	0.83[YRI][hapmap]
rs7938416	0.81[CEU][hapmap];0.96[YRI][hapmap];0.87[AFR][1000 genomes]
rs7952474	0.92[YRI][hapmap];0.86[AFR][1000 genomes]
rs9326313	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv556131	chr11:100985777-101480017	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv530644	chr11:101010088-101486038	Strong transcription Weak transcription Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv898330	chr11:101243644-101722031	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
4	esv2830219	chr11:101319531-101382967	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv976474	chr11:101364853-101369234	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101337800-101368200	Weak transcription	Ovary	ovary
2	chr11:101350000-101384800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr11:101359000-101372200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr11:101360000-101369000	Weak transcription	NHDF-Ad	bronchial
5	chr11:101362400-101373400	Weak transcription	Fetal Lung	lung
6	chr11:101363400-101369600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links