Variant report

Variant	rs10898214
Chromosome Location	chr11:83927158-83927159
allele	C/G
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:78)

rs_ID	r²[population]
rs10128587	0.90[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs1022308	0.90[CHB][hapmap];0.93[CHD][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs1040131	0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs10751105	0.80[CHB][hapmap];0.86[CHD][hapmap];0.82[GIH][hapmap];0.94[JPT][hapmap];0.83[MEX][hapmap];0.90[TSI][hapmap]
rs10751106	0.94[JPT][hapmap]
rs10751109	0.85[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs10751110	0.86[ASN][1000 genomes]
rs10751112	0.86[ASN][1000 genomes]
rs10792727	0.80[CHB][hapmap];0.88[JPT][hapmap]
rs10792728	0.80[CHB][hapmap]
rs10792731	0.94[ASW][hapmap];0.90[CHD][hapmap];0.82[GIH][hapmap];0.94[JPT][hapmap];0.96[YRI][hapmap]
rs10792740	0.90[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs10792742	0.90[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs10792744	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs10792745	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs10792746	0.90[CHB][hapmap];0.82[JPT][hapmap]
rs10898215	0.90[CHB][hapmap];0.93[CHD][hapmap];0.94[JPT][hapmap];0.83[MEX][hapmap];0.89[MKK][hapmap];0.84[YRI][hapmap];0.86[ASN][1000 genomes]
rs10898216	0.87[ASN][1000 genomes]
rs10898217	0.86[ASN][1000 genomes]
rs10898218	0.86[ASN][1000 genomes]
rs10898219	0.85[ASN][1000 genomes]
rs10898222	0.85[CHB][hapmap];0.81[JPT][hapmap]
rs11233953	0.90[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs11233954	0.90[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs11233956	0.90[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11233963	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs11233967	0.81[CHB][hapmap]
rs12278134	0.85[CHB][hapmap];0.84[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs12281587	0.90[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs1349820	0.83[CHD][hapmap];0.94[JPT][hapmap];0.83[MEX][hapmap]
rs1377746	0.80[CHB][hapmap];0.89[JPT][hapmap]
rs1377747	0.80[CHB][hapmap];0.89[JPT][hapmap]
rs1377748	0.88[ASW][hapmap];0.83[CHD][hapmap];0.82[GIH][hapmap];0.94[JPT][hapmap];0.80[LWK][hapmap];0.81[TSI][hapmap];0.81[AFR][1000 genomes]
rs1399617	0.95[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.81[MKK][hapmap];0.84[ASN][1000 genomes]
rs1399618	0.85[CHB][hapmap];0.84[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs1454021	0.90[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs1454023	0.90[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.87[ASN][1000 genomes]
rs1454026	0.94[JPT][hapmap]
rs1515084	0.80[CHB][hapmap];0.86[CHD][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs1515091	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1515092	0.85[CHB][hapmap];0.82[JPT][hapmap]
rs1515094	0.85[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs1551334	0.80[CHB][hapmap]
rs1573572	0.80[CHB][hapmap];0.88[JPT][hapmap]
rs1793037	0.80[CHB][hapmap];0.89[JPT][hapmap]
rs1793038	0.80[CHB][hapmap]
rs1793039	0.80[CHB][hapmap];0.83[JPT][hapmap]
rs1849877	0.90[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs1869470	0.90[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];0.88[MKK][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1869471	0.90[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs1869472	0.80[CHB][hapmap];0.88[JPT][hapmap]
rs1901973	0.86[ASN][1000 genomes]
rs2156848	0.94[JPT][hapmap]
rs2374526	0.85[ASN][1000 genomes]
rs4354715	0.90[CHB][hapmap];0.93[CHD][hapmap];0.94[JPT][hapmap];0.84[YRI][hapmap];0.84[ASN][1000 genomes]
rs4547116	0.82[MEX][hapmap]
rs4943889	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs4944471	0.80[CHD][hapmap];0.94[JPT][hapmap]
rs4944472	0.83[CHD][hapmap];0.94[JPT][hapmap]
rs4944474	0.86[ASN][1000 genomes]
rs7103429	0.89[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs7106175	0.90[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs7112322	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7120366	0.87[ASN][1000 genomes]
rs7122248	0.90[CHB][hapmap];0.82[JPT][hapmap]
rs7130225	0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs73519747	0.87[ASN][1000 genomes]
rs7483548	0.85[CHB][hapmap];0.88[JPT][hapmap]
rs7925243	0.82[ASW][hapmap];0.90[CHB][hapmap];0.93[CHD][hapmap];0.94[JPT][hapmap];0.87[LWK][hapmap];0.83[MEX][hapmap];0.87[MKK][hapmap];0.88[YRI][hapmap];0.82[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs7933566	0.85[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.83[ASN][1000 genomes]
rs7937925	0.85[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs7941004	0.94[JPT][hapmap];0.85[YRI][hapmap]
rs7943267	0.89[JPT][hapmap]
rs896996	0.85[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs896997	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs930790	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs963259	0.90[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.85[MKK][hapmap];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs988322	0.89[JPT][hapmap]

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	nsv1039924	chr11:83662904-83993497	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv541102	chr11:83662904-83993497	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv898029	chr11:83717887-83939591	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv948410	chr11:83918339-84812001	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv415	chr11:83924941-83969603	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83924200-83935000	Weak transcription	Brain Hippocampus Middle	brain
2	chr11:83926600-83927200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links