Variant report

Variant	rs34689326
Chromosome Location	chr3:97937023-97937024
allele	CA/TC
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 100 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1024056	0.81[AMR][1000 genomes]
rs11706357	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs11706390	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11715052	0.81[AMR][1000 genomes]
rs11715921	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11718318	0.81[AMR][1000 genomes]
rs11719161	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11720006	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11720576	0.80[AMR][1000 genomes]
rs11914600	0.81[AMR][1000 genomes]
rs11923541	0.81[AMR][1000 genomes]
rs12489167	0.82[AMR][1000 genomes]
rs13081420	0.81[AMR][1000 genomes]
rs13088168	0.81[AMR][1000 genomes]
rs13433847	0.81[AMR][1000 genomes]
rs1391151	0.81[AMR][1000 genomes]
rs1532463	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1532464	0.81[ASN][1000 genomes]
rs1532465	0.81[AMR][1000 genomes]
rs1587280	0.81[AMR][1000 genomes]
rs16839400	0.80[AMR][1000 genomes]
rs16839434	0.81[AMR][1000 genomes]
rs16839438	0.81[AMR][1000 genomes]
rs1846078	0.81[AMR][1000 genomes]
rs1908997	0.81[AMR][1000 genomes]
rs1908998	0.81[AMR][1000 genomes]
rs1908999	0.81[AMR][1000 genomes]
rs2047390	0.81[AMR][1000 genomes]
rs2047392	0.81[AMR][1000 genomes]
rs2047393	0.81[AMR][1000 genomes]
rs2088408	0.81[AMR][1000 genomes]
rs2316299	0.81[AMR][1000 genomes]
rs2316300	0.81[AMR][1000 genomes]
rs28481861	0.80[AMR][1000 genomes]
rs28484994	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs28678410	0.81[AMR][1000 genomes]
rs2873120	0.81[AMR][1000 genomes]
rs2873121	0.81[AMR][1000 genomes]
rs34111209	0.82[AMR][1000 genomes]
rs34573833	0.81[AMR][1000 genomes]
rs34826958	0.81[ASN][1000 genomes]
rs34918234	0.82[AMR][1000 genomes]
rs35122376	0.81[AMR][1000 genomes]
rs35200215	0.81[AMR][1000 genomes]
rs35327048	0.80[AMR][1000 genomes]
rs35907125	0.81[AMR][1000 genomes]
rs4264769	0.81[AMR][1000 genomes]
rs4286458	0.81[AMR][1000 genomes]
rs4452365	0.81[AMR][1000 genomes]
rs4463010	0.81[AMR][1000 genomes]
rs4463011	0.81[AMR][1000 genomes]
rs4464499	0.81[AMR][1000 genomes]
rs4482695	0.81[AMR][1000 genomes]
rs4550855	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4624601	0.81[AMR][1000 genomes]
rs4857345	0.81[AMR][1000 genomes]
rs4857346	0.81[AMR][1000 genomes]
rs4857347	0.81[AMR][1000 genomes]
rs4857348	0.81[AMR][1000 genomes]
rs4857351	0.81[ASN][1000 genomes]
rs5000372	0.81[AMR][1000 genomes]
rs5000373	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs5000376	0.83[AMR][1000 genomes]
rs5000377	0.83[AMR][1000 genomes]
rs62267190	0.81[AMR][1000 genomes]
rs62267191	0.81[AMR][1000 genomes]
rs6766382	0.82[ASN][1000 genomes]
rs6766681	0.81[AMR][1000 genomes]
rs6771099	0.81[AMR][1000 genomes]
rs6802178	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7430016	0.82[AMR][1000 genomes]
rs7633244	0.81[ASN][1000 genomes]
rs7634043	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7634063	0.81[AMR][1000 genomes]
rs7634274	0.81[AMR][1000 genomes]
rs7634735	0.81[AMR][1000 genomes]
rs7640900	0.80[ASN][1000 genomes]
rs7645384	0.81[AMR][1000 genomes]
rs7645400	0.81[AMR][1000 genomes]
rs7647986	0.81[AMR][1000 genomes]
rs9840421	0.81[AMR][1000 genomes]
rs9853761	0.80[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869347	chr3:97742604-98051633	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv877209	chr3:97806616-98049409	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv963576	chr3:97825434-98041343	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1004820	chr3:97852875-98169488	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv834773	chr3:97855362-98043888	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1000834	chr3:97859880-98095473	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv877210	chr3:97866177-97992964	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
8	esv13127	chr3:97899419-97939393	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv870074	chr3:97903273-97948850	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	esv2763288	chr3:97908670-97947253	Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Strong transcription	TF binding region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv432462	chr3:97918267-98001710	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
12	nsv877211	chr3:97919363-97958280	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv591063	chr3:97924688-97958280	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv591064	chr3:97931105-97958280	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region lncRNA	4 gene(s)	inside rSNPs	diseases
15	nsv877212	chr3:97931105-98033400	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
16	nsv520979	chr3:97934241-97937045	Weak transcription Enhancers	TF binding region	1 gene(s)	inside rSNPs	n/a
17	esv1842860	chr3:97934241-98075543	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
18	nsv1004762	chr3:97935701-98000227	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr3:97933800-97938000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr3:97936800-97937600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr3:97936800-97937800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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