Variant report

Variant	rs4282034
Chromosome Location	chr3:111926105-111926106
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 116 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:113)

rs_ID	r²[population]
rs1032398	0.87[ASW][hapmap];0.91[CHB][hapmap];0.81[JPT][hapmap];0.81[LWK][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs10934141	0.88[ASN][1000 genomes]
rs10934145	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs10934151	0.86[ASN][1000 genomes]
rs10934152	0.86[ASN][1000 genomes]
rs10934162	0.90[CHB][hapmap];0.89[JPT][hapmap]
rs11707558	0.92[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs11922559	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs11923778	0.92[CHB][hapmap]
rs12487206	0.87[ASN][1000 genomes]
rs12488760	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs12491362	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs12634742	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs12634769	0.92[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs12637609	1.00[CHB][hapmap];0.88[ASN][1000 genomes]
rs1304787	0.86[ASN][1000 genomes]
rs13080158	0.85[ASN][1000 genomes]
rs13081485	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs13081935	0.92[CHB][hapmap];0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs13082509	0.92[CHB][hapmap];0.90[JPT][hapmap]
rs13087086	0.92[CHB][hapmap];0.90[JPT][hapmap]
rs13091454	0.90[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs13100724	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs1492491	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16859207	0.82[CHB][hapmap]
rs16859355	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17446744	0.92[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs1826392	0.85[ASN][1000 genomes]
rs340164	0.82[CHB][hapmap]
rs4234412	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs4234413	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs4234415	0.82[ASN][1000 genomes]
rs4264699	0.86[ASN][1000 genomes]
rs4276157	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs4280609	0.86[ASN][1000 genomes]
rs4282033	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs4299459	0.89[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs4300982	0.91[CHB][hapmap];0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs4345043	0.86[ASN][1000 genomes]
rs4392388	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs4398404	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs4401342	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs4420835	0.85[ASN][1000 genomes]
rs4423739	0.86[ASN][1000 genomes]
rs4429601	0.86[ASN][1000 genomes]
rs4434124	0.86[ASN][1000 genomes]
rs4435608	0.86[ASN][1000 genomes]
rs4450779	0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4478055	0.82[ASN][1000 genomes]
rs4479562	0.86[ASN][1000 genomes]
rs4505669	0.92[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs4530500	0.86[ASN][1000 genomes]
rs4560270	0.92[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4560274	0.86[ASN][1000 genomes]
rs4568108	0.86[ASN][1000 genomes]
rs4571212	0.86[ASN][1000 genomes]
rs4572740	0.92[CHB][hapmap];0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs4580518	0.86[ASN][1000 genomes]
rs4585166	0.92[CHB][hapmap];0.90[JPT][hapmap]
rs4591478	0.86[ASN][1000 genomes]
rs4597682	0.86[ASN][1000 genomes]
rs4611789	0.92[CHB][hapmap];0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs4632517	0.92[CHB][hapmap];0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs4682096	0.86[ASN][1000 genomes]
rs4682097	0.92[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs4682380	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs4682382	0.86[ASN][1000 genomes]
rs55735606	0.88[ASN][1000 genomes]
rs56335531	0.87[ASN][1000 genomes]
rs59043683	0.92[AFR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs59967068	0.86[ASN][1000 genomes]
rs62276970	0.86[ASN][1000 genomes]
rs6438061	0.86[ASN][1000 genomes]
rs6438062	0.86[ASN][1000 genomes]
rs6773916	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs6781344	0.92[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs6788397	0.86[ASN][1000 genomes]
rs6791182	0.89[ASW][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.81[JPT][hapmap];0.85[ASN][1000 genomes]
rs6796949	0.86[ASN][1000 genomes]
rs6798551	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs6798665	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73853382	0.89[ASN][1000 genomes]
rs7613061	0.92[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs7616261	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs7624367	0.92[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs7625173	0.84[CHB][hapmap];0.86[CHD][hapmap]
rs7627314	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs7635054	0.86[ASN][1000 genomes]
rs7635069	0.86[ASN][1000 genomes]
rs7635156	0.86[ASN][1000 genomes]
rs7638520	0.92[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs9288946	0.82[ASN][1000 genomes]
rs9288947	0.80[ASN][1000 genomes]
rs9758396	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs9809384	0.92[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs9809404	0.92[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs9809696	0.85[ASN][1000 genomes]
rs9813794	0.86[ASN][1000 genomes]
rs9822786	0.92[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs9823421	0.92[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs9826043	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs9847574	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs9858911	0.86[ASN][1000 genomes]
rs9860819	0.92[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs9863061	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs9865494	0.85[ASN][1000 genomes]
rs9865784	0.86[ASN][1000 genomes]
rs9869657	0.88[ASN][1000 genomes]
rs9870132	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs9873623	0.86[ASN][1000 genomes]
rs9878213	0.92[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs9878675	0.86[ASN][1000 genomes]
rs9879184	0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv10307	chr3:111903974-112087686	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv591291	chr3:111914624-111962851	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
3	nsv591292	chr3:111914624-111993915	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111913200-111930000	Weak transcription	Left Ventricle	heart

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