Variant report

Variant	rs10982991
Chromosome Location	chr9:118660258-118660259
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10448252	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10817838	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10982941	0.81[EUR][1000 genomes]
rs10982942	0.81[EUR][1000 genomes]
rs10982952	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10982953	0.83[EUR][1000 genomes]
rs10982957	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10982967	0.87[ASN][1000 genomes]
rs10982968	0.85[EUR][1000 genomes]
rs10982970	0.85[EUR][1000 genomes]
rs10982976	1.00[EUR][1000 genomes]
rs10982978	1.00[EUR][1000 genomes]
rs10982979	1.00[EUR][1000 genomes]
rs10982981	1.00[EUR][1000 genomes]
rs10982982	0.82[CHB][hapmap];1.00[EUR][1000 genomes]
rs10982983	0.82[CHB][hapmap];1.00[EUR][1000 genomes]
rs10982984	0.82[CHB][hapmap];1.00[EUR][1000 genomes]
rs10982985	1.00[EUR][1000 genomes]
rs10982988	0.82[CHB][hapmap];1.00[EUR][1000 genomes]
rs10982996	1.00[EUR][1000 genomes]
rs10982997	0.82[CHB][hapmap]
rs10983000	1.00[EUR][1000 genomes]
rs10983003	0.98[EUR][1000 genomes]
rs10983004	0.98[EUR][1000 genomes]
rs10983005	0.98[EUR][1000 genomes]
rs10983007	0.98[EUR][1000 genomes]
rs12156496	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs12378638	1.00[EUR][1000 genomes]
rs12378736	0.82[CHB][hapmap];1.00[EUR][1000 genomes]
rs12380105	1.00[EUR][1000 genomes]
rs1243	0.82[CHB][hapmap];1.00[EUR][1000 genomes]
rs2040485	1.00[EUR][1000 genomes]
rs2418420	0.85[EUR][1000 genomes]
rs2418424	1.00[CHB][hapmap]
rs3761841	0.82[CHB][hapmap];1.00[EUR][1000 genomes]
rs3789264	0.98[EUR][1000 genomes]
rs4145478	1.00[EUR][1000 genomes]
rs62575660	1.00[EUR][1000 genomes]
rs62575661	1.00[EUR][1000 genomes]
rs62575662	1.00[EUR][1000 genomes]
rs62575664	1.00[EUR][1000 genomes]
rs62575665	0.98[EUR][1000 genomes]
rs62577089	0.81[EUR][1000 genomes]
rs62577091	1.00[AFR][1000 genomes]
rs62577094	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs62577095	0.86[AFR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62577110	0.83[EUR][1000 genomes]
rs62577130	0.85[EUR][1000 genomes]
rs62577137	1.00[EUR][1000 genomes]
rs62577138	1.00[EUR][1000 genomes]
rs62577139	1.00[EUR][1000 genomes]
rs62577140	1.00[EUR][1000 genomes]
rs62577141	1.00[EUR][1000 genomes]
rs62577142	1.00[EUR][1000 genomes]
rs62577143	1.00[EUR][1000 genomes]
rs62577146	1.00[EUR][1000 genomes]
rs62577147	1.00[EUR][1000 genomes]
rs62577148	1.00[EUR][1000 genomes]
rs62577150	1.00[EUR][1000 genomes]
rs62577151	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62577152	1.00[EUR][1000 genomes]
rs7024074	0.82[CHB][hapmap];1.00[EUR][1000 genomes]
rs7029447	1.00[EUR][1000 genomes]
rs7046862	0.82[CHB][hapmap];1.00[EUR][1000 genomes]
rs7047141	1.00[EUR][1000 genomes]
rs72616610	1.00[EUR][1000 genomes]
rs72616612	1.00[EUR][1000 genomes]
rs72616613	1.00[EUR][1000 genomes]
rs72616614	1.00[EUR][1000 genomes]
rs72616615	1.00[EUR][1000 genomes]
rs7861033	0.85[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	nsv948346	chr9:118107565-118718197	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv1046948	chr9:118185587-118926891	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv916622	chr9:118206309-118952390	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv540207	chr9:118206311-118920304	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv491661	chr9:118206312-118802177	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv1050714	chr9:118619303-118690263	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:118647200-118678600	Weak transcription	Placenta	Placenta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links