Variant report

Variant	rs298759
Chromosome Location	chr3:164197863-164197864
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:164190398..164192515-chr3:164196627..164199488,2	K562	blood:

Extended variants
information (count: 158 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:146)

rs_ID	r²[population]
rs1073608	0.85[ASN][1000 genomes]
rs1084719	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1084721	0.83[ASN][1000 genomes]
rs13313898	0.89[ASN][1000 genomes]
rs13324218	0.89[ASN][1000 genomes]
rs1347398	0.83[ASN][1000 genomes]
rs1435048	0.85[ASN][1000 genomes]
rs1435049	0.85[ASN][1000 genomes]
rs1435050	0.89[ASN][1000 genomes]
rs1435051	0.89[ASN][1000 genomes]
rs1435052	0.89[ASN][1000 genomes]
rs1513445	0.83[ASN][1000 genomes]
rs1513450	0.85[ASN][1000 genomes]
rs1579577	0.85[ASN][1000 genomes]
rs1579578	0.85[ASN][1000 genomes]
rs1579579	0.85[ASN][1000 genomes]
rs1579580	0.85[ASN][1000 genomes]
rs1600082	0.85[ASN][1000 genomes]
rs1606520	0.85[ASN][1000 genomes]
rs1606521	0.85[ASN][1000 genomes]
rs1611924	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1615363	0.85[ASN][1000 genomes]
rs1616240	0.84[ASN][1000 genomes]
rs1623011	0.83[ASN][1000 genomes]
rs1626432	0.85[ASN][1000 genomes]
rs1656094	0.85[ASN][1000 genomes]
rs1656096	0.85[ASN][1000 genomes]
rs1656097	0.85[ASN][1000 genomes]
rs1656098	0.85[ASN][1000 genomes]
rs1656099	0.85[ASN][1000 genomes]
rs1656109	0.85[ASN][1000 genomes]
rs1656110	0.85[ASN][1000 genomes]
rs1656111	0.85[ASN][1000 genomes]
rs1656113	0.85[ASN][1000 genomes]
rs1656114	0.85[ASN][1000 genomes]
rs1656115	0.85[ASN][1000 genomes]
rs1656116	0.85[ASN][1000 genomes]
rs1708469	0.85[ASN][1000 genomes]
rs1708470	0.85[ASN][1000 genomes]
rs1708471	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1708472	0.85[ASN][1000 genomes]
rs1708477	0.83[ASN][1000 genomes]
rs1708482	0.85[ASN][1000 genomes]
rs1708484	0.85[ASN][1000 genomes]
rs1708485	0.85[ASN][1000 genomes]
rs1708486	0.85[ASN][1000 genomes]
rs1708488	0.85[ASN][1000 genomes]
rs1708489	0.85[ASN][1000 genomes]
rs1708490	0.85[ASN][1000 genomes]
rs1708491	0.85[ASN][1000 genomes]
rs1708492	0.85[ASN][1000 genomes]
rs1708493	0.85[ASN][1000 genomes]
rs1708494	0.85[ASN][1000 genomes]
rs1708497	0.90[ASN][1000 genomes]
rs1708498	0.85[ASN][1000 genomes]
rs1708501	0.84[ASN][1000 genomes]
rs1708502	0.85[ASN][1000 genomes]
rs1708503	0.85[ASN][1000 genomes]
rs1708504	0.84[ASN][1000 genomes]
rs1708505	0.85[ASN][1000 genomes]
rs2117533	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2117535	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2117536	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2141852	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2181	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2182	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2304377	0.89[ASN][1000 genomes]
rs28421950	0.83[ASN][1000 genomes]
rs2886570	0.87[ASN][1000 genomes]
rs298741	0.85[ASN][1000 genomes]
rs298742	0.85[ASN][1000 genomes]
rs298743	0.85[ASN][1000 genomes]
rs298744	0.85[ASN][1000 genomes]
rs298745	0.85[ASN][1000 genomes]
rs298746	0.86[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs298747	0.86[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs298755	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs298756	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs298757	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs298758	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs298760	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs367230	0.85[ASN][1000 genomes]
rs378206	0.85[ASN][1000 genomes]
rs3816090	0.89[ASN][1000 genomes]
rs393334	0.93[ASN][1000 genomes]
rs401402	0.85[ASN][1000 genomes]
rs410229	0.84[ASN][1000 genomes]
rs419649	0.84[ASN][1000 genomes]
rs420836	0.85[ASN][1000 genomes]
rs433861	0.85[ASN][1000 genomes]
rs434335	0.85[ASN][1000 genomes]
rs442287	0.85[ASN][1000 genomes]
rs452224	0.85[ASN][1000 genomes]
rs4855177	0.86[ASN][1000 genomes]
rs4855247	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs66465044	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs66685021	0.80[ASN][1000 genomes]
rs66949604	0.87[ASN][1000 genomes]
rs67216762	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs67336409	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs73157132	0.80[ASN][1000 genomes]
rs7612403	0.85[ASN][1000 genomes]
rs7617240	0.80[ASN][1000 genomes]
rs7618193	0.89[ASN][1000 genomes]
rs7623330	0.85[ASN][1000 genomes]
rs7623591	0.85[ASN][1000 genomes]
rs7625665	0.85[ASN][1000 genomes]
rs7626138	0.85[ASN][1000 genomes]
rs7636354	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7637477	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7638296	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7638502	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7639917	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7639997	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7640767	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7648537	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7650970	0.89[ASN][1000 genomes]
rs7651057	0.89[ASN][1000 genomes]
rs783583	0.83[ASN][1000 genomes]
rs783584	0.83[ASN][1000 genomes]
rs783585	0.83[ASN][1000 genomes]
rs783586	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs783587	0.83[ASN][1000 genomes]
rs783589	0.83[ASN][1000 genomes]
rs811459	0.83[ASN][1000 genomes]
rs811955	0.84[ASN][1000 genomes]
rs811956	0.83[ASN][1000 genomes]
rs814147	0.83[ASN][1000 genomes]
rs9290232	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9835203	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9835359	0.83[ASN][1000 genomes]
rs9835558	0.86[ASN][1000 genomes]
rs9835718	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9839722	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9840047	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9840091	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9844292	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9844690	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9855296	0.85[ASN][1000 genomes]
rs9864025	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9864184	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9873142	0.85[ASN][1000 genomes]
rs9876091	0.85[ASN][1000 genomes]
rs9882072	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs997207	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs999592	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009069	chr3:163787128-164323219	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv877840	chr3:163832988-164200220	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1010490	chr3:163961100-164399225	Enhancers Strong transcription ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv497973	chr3:163970658-164370204	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1014815	chr3:164007081-164359622	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv877893	chr3:164018044-164202045	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	esv1843213	chr3:164018044-164209573	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv1006002	chr3:164021906-164653572	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv998340	chr3:164047951-164325380	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv999285	chr3:164133483-164326560	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv536791	chr3:164133483-164326560	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	esv2763323	chr3:164189618-164243301	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	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	chr3:164195200-164202200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr3:164197000-164198000	Enhancers	Liver	Liver
3	chr3:164197600-164198400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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