Variant report

Variant	rs6784648
Chromosome Location	chr3:110223311-110223312
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:110222894..110225675-chr3:110240158..110242098,2	K562	blood:
2	chr3:110223100..110226514-chr3:110228942..110230704,3	K562	blood:
3	chr3:110223081..110225312-chr3:110255969..110257984,2	K562	blood:
4	chr3:110195963..110198828-chr3:110223194..110225023,2	K562	blood:

Extended variants
information (count: 126 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:115)

rs_ID	r²[population]
rs1028026	0.86[ASN][1000 genomes]
rs1028027	0.86[ASN][1000 genomes]
rs10934045	0.83[ASN][1000 genomes]
rs10934046	0.81[ASN][1000 genomes]
rs12054102	0.90[EUR][1000 genomes]
rs12487462	0.90[JPT][hapmap];0.81[ASN][1000 genomes]
rs13062461	0.84[ASN][1000 genomes]
rs13093393	0.80[ASN][1000 genomes]
rs1398346	0.90[CHB][hapmap];0.90[JPT][hapmap];0.87[ASN][1000 genomes]
rs1398348	0.81[ASN][1000 genomes]
rs1398349	0.81[ASN][1000 genomes]
rs1398354	0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs1398409	0.81[ASN][1000 genomes]
rs1512519	0.81[ASN][1000 genomes]
rs1512540	0.83[ASN][1000 genomes]
rs1512660	0.83[ASN][1000 genomes]
rs1512661	0.83[ASN][1000 genomes]
rs1512662	0.84[EUR][1000 genomes]
rs1574700	0.83[ASN][1000 genomes]
rs1606349	0.81[ASN][1000 genomes]
rs1606350	0.84[EUR][1000 genomes]
rs16856690	0.83[EUR][1000 genomes]
rs16856946	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1849379	0.89[ASN][1000 genomes]
rs1913088	0.83[ASN][1000 genomes]
rs1913100	0.81[ASN][1000 genomes]
rs2055966	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs2055968	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2399335	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs2399336	0.81[ASN][1000 genomes]
rs2399337	0.82[ASN][1000 genomes]
rs2895375	0.84[EUR][1000 genomes]
rs4682180	0.85[ASN][1000 genomes]
rs4682589	0.82[ASN][1000 genomes]
rs4682590	0.80[ASN][1000 genomes]
rs4682594	0.83[ASN][1000 genomes]
rs56067719	0.83[ASN][1000 genomes]
rs57198450	0.83[EUR][1000 genomes]
rs57680282	0.89[EUR][1000 genomes]
rs58500543	0.91[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59612531	0.83[EUR][1000 genomes]
rs59822825	0.83[EUR][1000 genomes]
rs59985710	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62269411	0.83[EUR][1000 genomes]
rs62269412	0.83[EUR][1000 genomes]
rs62269414	0.83[EUR][1000 genomes]
rs62269437	0.89[EUR][1000 genomes]
rs62269438	0.89[EUR][1000 genomes]
rs62269439	0.89[EUR][1000 genomes]
rs62270060	0.89[EUR][1000 genomes]
rs62270063	0.89[EUR][1000 genomes]
rs62270076	0.89[EUR][1000 genomes]
rs62270083	0.89[EUR][1000 genomes]
rs62270086	0.89[EUR][1000 genomes]
rs62270095	0.89[EUR][1000 genomes]
rs62270100	0.89[EUR][1000 genomes]
rs62270124	0.83[EUR][1000 genomes]
rs62270128	0.83[EUR][1000 genomes]
rs62270134	0.83[EUR][1000 genomes]
rs62271562	0.95[EUR][1000 genomes]
rs62271576	1.00[EUR][1000 genomes]
rs62271578	0.92[AFR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62271586	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62271587	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62271588	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62271591	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62271592	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62271606	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62271607	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62271608	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62271609	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62271610	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62271612	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62271615	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62271616	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62271618	0.89[EUR][1000 genomes]
rs62271620	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62271621	0.89[EUR][1000 genomes]
rs62271636	0.89[EUR][1000 genomes]
rs62271639	0.89[EUR][1000 genomes]
rs62271642	0.89[EUR][1000 genomes]
rs62271644	0.89[EUR][1000 genomes]
rs62271647	0.89[EUR][1000 genomes]
rs6437914	0.92[AFR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs67166271	0.81[ASN][1000 genomes]
rs6765569	0.89[EUR][1000 genomes]
rs6771696	0.80[ASN][1000 genomes]
rs6781483	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6784411	0.83[EUR][1000 genomes]
rs73217304	0.81[ASN][1000 genomes]
rs7613348	0.83[ASN][1000 genomes]
rs7616260	0.81[ASN][1000 genomes]
rs7617903	0.95[EUR][1000 genomes]
rs7627828	0.81[ASN][1000 genomes]
rs7628733	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7631316	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7634524	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs7640587	0.83[ASN][1000 genomes]
rs7640755	0.91[JPT][hapmap]
rs7640794	0.82[ASN][1000 genomes]
rs9653909	0.89[EUR][1000 genomes]
rs9809312	0.84[EUR][1000 genomes]
rs9813893	0.95[JPT][hapmap]
rs9815868	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs9826577	0.83[ASN][1000 genomes]
rs9831873	0.86[ASN][1000 genomes]
rs9843950	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs9846566	0.83[ASN][1000 genomes]
rs9860708	0.83[ASN][1000 genomes]
rs9867550	0.83[ASN][1000 genomes]
rs9872133	0.89[ASN][1000 genomes]
rs9872620	0.81[ASN][1000 genomes]
rs9877235	0.87[ASN][1000 genomes]
rs9877472	0.83[ASN][1000 genomes]
rs9877920	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999414	chr3:110103126-110340180	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv829670	chr3:110134650-110308256	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv520365	chr3:110155172-110441165	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1001144	chr3:110158316-110431113	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv536687	chr3:110158316-110431113	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1001810	chr3:110158316-110522247	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1010230	chr3:110204439-110588814	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv536688	chr3:110204439-110588814	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv829672	chr3:110206693-110361632	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv1011034	chr3:110209344-110559021	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv536689	chr3:110209344-110559021	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr3:110223200-110223800	Flanking Active TSS	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links