Variant report

Variant	rs6509019
Chromosome Location	chr19:43090253-43090254
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 98 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs10401178	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10401428	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10402245	1.00[MEX][hapmap];1.00[TSI][hapmap]
rs10403065	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10404589	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10405037	1.00[EUR][1000 genomes]
rs10405152	1.00[CEU][hapmap];0.93[YRI][hapmap];0.93[AMR][1000 genomes]
rs10405410	0.93[ASW][hapmap];1.00[CEU][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10405942	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10412074	1.00[EUR][1000 genomes]
rs10412594	1.00[EUR][1000 genomes]
rs10415284	1.00[EUR][1000 genomes]
rs10416108	1.00[CEU][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10418997	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10419543	1.00[EUR][1000 genomes]
rs10419561	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10420773	1.00[EUR][1000 genomes]
rs10422191	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10423370	1.00[EUR][1000 genomes]
rs10424206	1.00[CEU][hapmap];0.93[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10425119	1.00[CEU][hapmap]
rs10425199	1.00[EUR][1000 genomes]
rs10425666	1.00[EUR][1000 genomes]
rs10426304	1.00[EUR][1000 genomes]
rs11878991	1.00[CEU][hapmap]
rs11879033	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11880554	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];1.00[EUR][1000 genomes]
rs11880876	1.00[EUR][1000 genomes]
rs11881583	1.00[CEU][hapmap];0.93[YRI][hapmap];0.87[AMR][1000 genomes]
rs11882225	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11882701	0.93[AMR][1000 genomes]
rs11883425	1.00[CEU][hapmap]
rs13343840	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13345272	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13345659	1.00[TSI][hapmap]
rs13346522	1.00[EUR][1000 genomes]
rs16975750	1.00[MEX][hapmap];1.00[TSI][hapmap]
rs16975799	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.93[AMR][1000 genomes]
rs16975862	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2051832	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2051833	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs28425201	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28473486	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28588100	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28602626	1.00[EUR][1000 genomes]
rs28625452	0.93[AMR][1000 genomes]
rs28635141	1.00[EUR][1000 genomes]
rs28660279	1.00[EUR][1000 genomes]
rs41348545	1.00[EUR][1000 genomes]
rs41381546	1.00[EUR][1000 genomes]
rs41421250	1.00[EUR][1000 genomes]
rs60747186	0.83[EUR][1000 genomes]
rs61388144	1.00[EUR][1000 genomes]
rs6509015	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];1.00[EUR][1000 genomes]
rs7245385	1.00[MEX][hapmap];1.00[TSI][hapmap]
rs7246161	1.00[CEU][hapmap]
rs7246591	1.00[CEU][hapmap]
rs7247278	1.00[CEU][hapmap];0.83[YRI][hapmap];1.00[EUR][1000 genomes]
rs7250501	1.00[EUR][1000 genomes]
rs7251638	1.00[TSI][hapmap]
rs7252874	0.88[AMR][1000 genomes]
rs7253634	1.00[EUR][1000 genomes]
rs7255271	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7256226	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7256850	1.00[EUR][1000 genomes]
rs7258854	1.00[CEU][hapmap]
rs7259335	1.00[EUR][1000 genomes]
rs73558492	1.00[EUR][1000 genomes]
rs73558498	1.00[EUR][1000 genomes]
rs73560408	1.00[EUR][1000 genomes]
rs8104731	0.93[AMR][1000 genomes]
rs8105525	0.87[ASW][hapmap];1.00[CEU][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];1.00[EUR][1000 genomes]
rs8106836	1.00[EUR][1000 genomes]
rs8108992	1.00[EUR][1000 genomes]
rs8110904	0.83[YRI][hapmap];1.00[EUR][1000 genomes]
rs8111171	1.00[EUR][1000 genomes]
rs8112593	1.00[EUR][1000 genomes]
rs8112915	1.00[EUR][1000 genomes]
rs8113154	1.00[EUR][1000 genomes]
rs8113448	1.00[EUR][1000 genomes]
rs9749434	1.00[EUR][1000 genomes]
rs9917002	0.93[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526186	chr19:42676481-43203507	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
2	esv2422471	chr19:42733141-43669485	Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
3	esv2422468	chr19:42991289-43669027	Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1057390	chr19:43003323-43173028	Enhancers Genic enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv482597	chr19:43037214-43222644	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv2758501	chr19:43042747-43899053	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
7	esv2758763	chr19:43042747-43899053	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
8	nsv428023	chr19:43042747-43899053	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
9	esv2422227	chr19:43059426-43669485	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
10	esv3439256	chr19:43065661-43098816	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	esv3360773	chr19:43065661-43137022	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv1064734	chr19:43076046-43182478	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv978823	chr19:43081358-43094705	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
14	nsv1058936	chr19:43082848-43228161	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
15	nsv482221	chr19:43084395-43099082	Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
16	esv3331281	chr19:43087545-43124628	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43081400-43100600	Weak transcription	Spleen	Spleen
2	chr19:43088000-43092200	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr19:43090200-43091200	Bivalent Enhancer	Primary B cells from cord blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links