Variant report

Variant	rs1317774
Chromosome Location	chr8:52635679-52635680
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10090123	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10090972	0.92[EUR][1000 genomes]
rs10091454	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10106091	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10109862	0.84[EUR][1000 genomes]
rs10958295	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10958296	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10958297	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12548147	0.81[EUR][1000 genomes]
rs13251959	0.82[EUR][1000 genomes]
rs13251960	0.91[EUR][1000 genomes]
rs13268396	0.83[EUR][1000 genomes]
rs13268711	0.84[EUR][1000 genomes]
rs13270001	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13274101	0.83[EUR][1000 genomes]
rs13277004	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13279413	0.91[EUR][1000 genomes]
rs16916741	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16916756	0.84[EUR][1000 genomes]
rs16916763	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28512421	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28549751	0.91[EUR][1000 genomes]
rs28616568	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2976209	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34342438	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35153909	0.83[EUR][1000 genomes]
rs35195931	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs36052716	0.81[EUR][1000 genomes]
rs36075262	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4242470	0.81[EUR][1000 genomes]
rs4242472	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4275221	0.84[EUR][1000 genomes]
rs4326377	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4397396	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4400372	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4873201	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4873572	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4873573	0.83[EUR][1000 genomes]
rs4873575	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4873584	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs55701628	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6981260	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6986571	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6986605	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6999693	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7005788	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7007671	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7007804	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7011666	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7839661	0.92[EUR][1000 genomes]
rs9643788	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9650303	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932026	chr8:51858658-52758574	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv817615	chr8:52252405-53023384	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1018429	chr8:52411443-52878946	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv1034856	chr8:52411443-52886765	Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv831313	chr8:52458835-52638968	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv890898	chr8:52579964-52680933	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:52630600-52636000	Weak transcription	Pancreas	Pancrea
2	chr8:52633800-52636400	Weak transcription	Right Ventricle	heart
3	chr8:52634400-52637400	Enhancers	Left Ventricle	heart
4	chr8:52635200-52636200	Weak transcription	Right Atrium	heart
5	chr8:52635200-52639000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links