Variant report

Variant	rs9582137
Chromosome Location	chr13:98136598-98136599
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10161693	0.87[AMR][1000 genomes]
rs12100323	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12184576	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs13378459	0.87[AMR][1000 genomes]
rs13378494	1.00[EUR][1000 genomes]
rs16954162	1.00[EUR][1000 genomes]
rs184730	0.83[EUR][1000 genomes]
rs187012	0.83[EUR][1000 genomes]
rs2769284	0.83[EUR][1000 genomes]
rs2769285	0.83[EUR][1000 genomes]
rs2769288	0.83[EUR][1000 genomes]
rs2769290	0.83[EUR][1000 genomes]
rs2770217	0.83[EUR][1000 genomes]
rs2770218	0.83[EUR][1000 genomes]
rs2770223	0.83[EUR][1000 genomes]
rs2770228	0.83[EUR][1000 genomes]
rs34575456	0.94[EUR][1000 genomes]
rs349113	0.83[EUR][1000 genomes]
rs349117	0.83[EUR][1000 genomes]
rs349118	0.83[EUR][1000 genomes]
rs349119	0.83[EUR][1000 genomes]
rs349122	0.83[EUR][1000 genomes]
rs349124	0.83[EUR][1000 genomes]
rs349125	0.83[EUR][1000 genomes]
rs349126	0.83[EUR][1000 genomes]
rs384217	0.83[EUR][1000 genomes]
rs45560245	0.93[EUR][1000 genomes]
rs471754	0.83[EUR][1000 genomes]
rs55694844	0.83[EUR][1000 genomes]
rs56057629	0.83[EUR][1000 genomes]
rs57104501	0.83[EUR][1000 genomes]
rs57491525	0.83[EUR][1000 genomes]
rs59446249	0.83[EUR][1000 genomes]
rs60500694	0.93[EUR][1000 genomes]
rs7318655	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7331217	0.83[EUR][1000 genomes]
rs7331520	0.83[EUR][1000 genomes]
rs7331537	0.83[EUR][1000 genomes]
rs7335777	0.83[EUR][1000 genomes]
rs73564120	1.00[EUR][1000 genomes]
rs73564126	1.00[EUR][1000 genomes]
rs73564135	1.00[EUR][1000 genomes]
rs73564148	1.00[EUR][1000 genomes]
rs74105181	0.87[AMR][1000 genomes]
rs74105498	0.83[EUR][1000 genomes]
rs787468	0.83[EUR][1000 genomes]
rs9300411	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs9300412	1.00[CEU][hapmap];0.80[YRI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9300413	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9300418	0.83[EUR][1000 genomes]
rs9300424	0.83[EUR][1000 genomes]
rs9582132	0.93[EUR][1000 genomes]
rs9582133	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs9582134	0.93[EUR][1000 genomes]
rs9582135	1.00[CEU][hapmap];0.80[YRI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9582136	1.00[EUR][1000 genomes]
rs9582138	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9582139	0.87[EUR][1000 genomes]
rs9582141	0.83[EUR][1000 genomes]
rs9582144	1.00[EUR][1000 genomes]
rs9582147	0.93[EUR][1000 genomes]
rs9584567	0.87[AMR][1000 genomes]
rs9584575	0.80[YRI][hapmap];0.87[AMR][1000 genomes]
rs9584577	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9584578	1.00[CEU][hapmap];0.80[YRI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9584579	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs9584580	1.00[CEU][hapmap];0.80[YRI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9584581	0.80[YRI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9584582	0.93[EUR][1000 genomes]
rs9584583	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs9584592	0.83[EUR][1000 genomes]
rs9584595	1.00[EUR][1000 genomes]
rs9584596	1.00[EUR][1000 genomes]
rs9584597	0.83[EUR][1000 genomes]
rs9584598	1.00[EUR][1000 genomes]
rs9584599	1.00[EUR][1000 genomes]
rs9584600	0.94[EUR][1000 genomes]
rs9584615	1.00[EUR][1000 genomes]
rs9584626	0.94[EUR][1000 genomes]
rs9805408	0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832694	chr13:97930561-98137882	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
2	nsv1139	chr13:98133793-98178130	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1043113	chr13:98136208-98485012	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv541884	chr13:98136208-98485012	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:98135600-98137000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr13:98135800-98137400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr13:98136200-98137000	Enhancers	Fetal Lung	lung
4	chr13:98136200-98137000	Enhancers	Skeletal Muscle Female	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links