Variant report

Variant	rs6771673
Chromosome Location	chr3:17856860-17856861
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:17856634..17858275-chr3:17861153..17864050,2	K562	blood:
2	chr3:17850838..17853208-chr3:17856384..17858538,2	MCF-7	breast:

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs1004307	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10428260	0.81[EUR][1000 genomes]
rs11128857	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11128871	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12492504	0.81[EUR][1000 genomes]
rs12495352	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13062642	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13071301	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13076950	0.80[EUR][1000 genomes]
rs1430896	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1430904	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1469558	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17200916	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17200979	0.87[EUR][1000 genomes]
rs17273111	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2033373	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2033374	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2033376	0.82[AMR][1000 genomes]
rs2033377	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2033378	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2033379	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2337387	0.98[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28796017	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4243833	0.80[EUR][1000 genomes]
rs4243834	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4260468	0.85[ASN][1000 genomes]
rs4330281	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4422341	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4450852	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4632574	0.81[EUR][1000 genomes]
rs4908942	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4908976	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4908978	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4908979	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4908981	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4908982	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4908984	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4908985	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4908986	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4908988	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6577597	0.98[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6577598	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6780932	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6787380	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6794859	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6802932	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6804677	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7428585	0.80[EUR][1000 genomes]
rs7632834	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7633898	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs919562	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9862290	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999594	chr3:17690416-17982318	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:17851400-17861000	Weak transcription	Right Atrium	heart
2	chr3:17855800-17860600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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