Variant report

Variant	rs16859355
Chromosome Location	chr3:111951703-111951704
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs1032398	0.83[AFR][1000 genomes]
rs10934141	0.96[ASN][1000 genomes]
rs10934151	0.94[ASN][1000 genomes]
rs10934152	0.94[ASN][1000 genomes]
rs11707558	0.96[ASN][1000 genomes]
rs12487206	0.92[ASN][1000 genomes]
rs12491362	0.94[ASN][1000 genomes]
rs12634742	0.96[ASN][1000 genomes]
rs12634769	0.96[ASN][1000 genomes]
rs12637609	0.96[ASN][1000 genomes]
rs1304787	0.94[ASN][1000 genomes]
rs13080158	0.93[ASN][1000 genomes]
rs13081485	0.89[ASN][1000 genomes]
rs13081935	0.89[ASN][1000 genomes]
rs13091454	0.96[ASN][1000 genomes]
rs1492491	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17446744	0.96[ASN][1000 genomes]
rs1826392	0.92[ASN][1000 genomes]
rs4234415	0.89[ASN][1000 genomes]
rs4264699	0.94[ASN][1000 genomes]
rs4280609	0.94[ASN][1000 genomes]
rs4282034	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4299459	0.91[ASN][1000 genomes]
rs4300982	0.90[ASN][1000 genomes]
rs4345043	0.94[ASN][1000 genomes]
rs4420835	0.92[ASN][1000 genomes]
rs4423739	0.94[ASN][1000 genomes]
rs4429601	0.94[ASN][1000 genomes]
rs4434124	0.94[ASN][1000 genomes]
rs4435608	0.94[ASN][1000 genomes]
rs4450779	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4478055	0.89[ASN][1000 genomes]
rs4479562	0.94[ASN][1000 genomes]
rs4505669	0.94[ASN][1000 genomes]
rs4530500	0.94[ASN][1000 genomes]
rs4560270	0.93[ASN][1000 genomes]
rs4560274	0.94[ASN][1000 genomes]
rs4568108	0.94[ASN][1000 genomes]
rs4571212	0.94[ASN][1000 genomes]
rs4572740	0.89[ASN][1000 genomes]
rs4580518	0.94[ASN][1000 genomes]
rs4585166	0.86[ASN][1000 genomes]
rs4591478	0.94[ASN][1000 genomes]
rs4597682	0.94[ASN][1000 genomes]
rs4611789	0.89[ASN][1000 genomes]
rs4632517	0.89[ASN][1000 genomes]
rs4682096	0.94[ASN][1000 genomes]
rs4682097	0.94[ASN][1000 genomes]
rs4682382	0.94[ASN][1000 genomes]
rs55735606	0.96[ASN][1000 genomes]
rs56335531	0.95[ASN][1000 genomes]
rs59043683	0.94[AFR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59967068	0.94[ASN][1000 genomes]
rs62276970	0.94[ASN][1000 genomes]
rs6438061	0.94[ASN][1000 genomes]
rs6438062	0.94[ASN][1000 genomes]
rs6781344	0.96[ASN][1000 genomes]
rs6788397	0.94[ASN][1000 genomes]
rs6791182	0.92[ASN][1000 genomes]
rs6796949	0.94[ASN][1000 genomes]
rs6798665	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73853382	0.97[ASN][1000 genomes]
rs7613061	0.94[ASN][1000 genomes]
rs7624367	0.94[ASN][1000 genomes]
rs7635054	0.94[ASN][1000 genomes]
rs7635069	0.94[ASN][1000 genomes]
rs7635156	0.94[ASN][1000 genomes]
rs7638520	0.94[ASN][1000 genomes]
rs9288946	0.89[ASN][1000 genomes]
rs9288947	0.87[ASN][1000 genomes]
rs9809384	0.94[ASN][1000 genomes]
rs9809404	0.94[ASN][1000 genomes]
rs9809696	0.93[ASN][1000 genomes]
rs9813794	0.94[ASN][1000 genomes]
rs9822786	0.94[ASN][1000 genomes]
rs9823421	0.94[ASN][1000 genomes]
rs9858911	0.94[ASN][1000 genomes]
rs9860819	0.94[ASN][1000 genomes]
rs9865494	0.93[ASN][1000 genomes]
rs9865784	0.94[ASN][1000 genomes]
rs9869657	0.96[ASN][1000 genomes]
rs9870132	0.96[ASN][1000 genomes]
rs9873623	0.94[ASN][1000 genomes]
rs9878213	0.94[ASN][1000 genomes]
rs9878675	0.94[ASN][1000 genomes]
rs9879184	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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
4	nsv877340	chr3:111936961-112013546	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr3:111942400-111952400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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