Variant report

Variant	rs9814169
Chromosome Location	chr3:76101205-76101206
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs11917746	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12714847	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12714848	0.82[AMR][1000 genomes]
rs1471994	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1489090	0.85[AMR][1000 genomes]
rs1489091	0.84[AMR][1000 genomes]
rs1489092	0.83[AMR][1000 genomes]
rs1489093	0.87[AMR][1000 genomes]
rs1489096	0.87[AMR][1000 genomes]
rs1489097	0.87[AMR][1000 genomes]
rs1489098	0.81[AMR][1000 genomes]
rs1489099	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1968951	0.87[AMR][1000 genomes]
rs2171638	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2220458	0.85[AMR][1000 genomes]
rs2324470	0.81[AMR][1000 genomes]
rs2324471	0.81[AMR][1000 genomes]
rs4260451	0.87[AMR][1000 genomes]
rs4306863	0.89[AMR][1000 genomes]
rs4449327	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4484199	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4566540	0.84[AMR][1000 genomes]
rs4624567	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4855969	0.82[AMR][1000 genomes]
rs4856004	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6549831	0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6549832	0.85[AMR][1000 genomes]
rs6770732	0.82[ASN][1000 genomes]
rs6776686	0.87[AMR][1000 genomes]
rs6776915	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6778177	0.85[AMR][1000 genomes]
rs6778933	0.81[AMR][1000 genomes]
rs6779552	0.81[AMR][1000 genomes]
rs6780227	0.99[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6780479	0.85[AMR][1000 genomes]
rs6780798	0.85[AMR][1000 genomes]
rs6783384	0.82[AMR][1000 genomes]
rs6786288	0.82[ASN][1000 genomes]
rs6802647	0.81[AMR][1000 genomes]
rs7610010	0.86[AMR][1000 genomes]
rs7620001	0.86[AMR][1000 genomes]
rs7625148	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7653310	0.81[AMR][1000 genomes]
rs9754680	0.85[AMR][1000 genomes]
rs9755934	0.84[AMR][1000 genomes]
rs9755939	0.85[AMR][1000 genomes]
rs9812834	0.91[AMR][1000 genomes]
rs9824924	0.85[AMR][1000 genomes]
rs9833136	0.82[AMR][1000 genomes]
rs9833153	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9837726	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs9840618	0.81[AMR][1000 genomes]
rs9852030	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9853890	0.84[AMR][1000 genomes]
rs9879542	0.87[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	esv2763279	chr3:75958155-76107685	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv876995	chr3:76015252-76114539	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1012705	chr3:76047819-76276542	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv998038	chr3:76053664-76218646	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv536591	chr3:76053664-76218646	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1007586	chr3:76053664-76280612	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv979847	chr3:76058868-76143057	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv999868	chr3:76068393-76274977	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv869827	chr3:76074846-76142916	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv432458	chr3:76077110-76119510	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv2757876	chr3:76077290-76167295	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv518802	chr3:76083946-76101757	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv1009175	chr3:76084525-76103687	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv999298	chr3:76084525-76105554	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv876996	chr3:76094221-76131251	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv1004976	chr3:76098108-76218646	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:76095000-76111000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr3:76101200-76101400	Enhancers	HUES6 Cell Line	embryonic stem cell

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