Variant report

Variant	rs6826942
Chromosome Location	chr4:22370483-22370484
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 102 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs1061576	0.94[EUR][1000 genomes]
rs10938887	0.94[EUR][1000 genomes]
rs10938889	0.95[EUR][1000 genomes]
rs10938890	0.95[EUR][1000 genomes]
rs10938891	0.95[EUR][1000 genomes]
rs10938892	0.94[EUR][1000 genomes]
rs10938893	0.94[EUR][1000 genomes]
rs11722233	0.94[EUR][1000 genomes]
rs11724496	0.94[EUR][1000 genomes]
rs11728954	0.95[EUR][1000 genomes]
rs11728998	0.95[EUR][1000 genomes]
rs11729007	0.94[EUR][1000 genomes]
rs11731357	0.95[EUR][1000 genomes]
rs11731358	0.95[EUR][1000 genomes]
rs11731999	0.95[EUR][1000 genomes]
rs11736657	0.94[EUR][1000 genomes]
rs11945871	0.94[EUR][1000 genomes]
rs11945937	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11946982	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12108221	0.95[EUR][1000 genomes]
rs12642856	0.94[EUR][1000 genomes]
rs12645926	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12647479	0.94[EUR][1000 genomes]
rs12648584	0.96[EUR][1000 genomes]
rs13114428	0.91[EUR][1000 genomes]
rs13133620	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13139975	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1318890	0.94[EUR][1000 genomes]
rs1392598	0.95[EUR][1000 genomes]
rs1500457	0.94[EUR][1000 genomes]
rs1500460	0.94[EUR][1000 genomes]
rs1500461	0.94[EUR][1000 genomes]
rs1604141	0.95[EUR][1000 genomes]
rs1604142	0.95[EUR][1000 genomes]
rs16872568	0.93[EUR][1000 genomes]
rs1827238	0.95[EUR][1000 genomes]
rs1846733	0.94[EUR][1000 genomes]
rs1846734	0.94[EUR][1000 genomes]
rs2202025	0.92[ASN][1000 genomes]
rs2270851	0.95[EUR][1000 genomes]
rs2270852	0.95[EUR][1000 genomes]
rs2270853	0.95[EUR][1000 genomes]
rs2323479	0.94[EUR][1000 genomes]
rs4235297	0.84[EUR][1000 genomes]
rs4311299	0.94[EUR][1000 genomes]
rs4452414	0.95[EUR][1000 genomes]
rs4697008	0.94[EUR][1000 genomes]
rs4697009	0.94[EUR][1000 genomes]
rs4697010	0.94[EUR][1000 genomes]
rs4697287	0.84[EUR][1000 genomes]
rs4697290	0.95[EUR][1000 genomes]
rs4697291	0.95[EUR][1000 genomes]
rs55840807	0.95[EUR][1000 genomes]
rs55986313	0.93[EUR][1000 genomes]
rs6448152	0.96[EUR][1000 genomes]
rs66517241	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs66891779	0.96[EUR][1000 genomes]
rs67201921	0.95[EUR][1000 genomes]
rs6824528	0.96[EUR][1000 genomes]
rs6824899	0.95[EUR][1000 genomes]
rs6824974	0.94[EUR][1000 genomes]
rs6826620	0.95[EUR][1000 genomes]
rs6829980	0.94[EUR][1000 genomes]
rs6830189	0.94[EUR][1000 genomes]
rs6852219	0.95[EUR][1000 genomes]
rs6852389	0.95[EUR][1000 genomes]
rs6852417	0.94[EUR][1000 genomes]
rs6853112	0.94[EUR][1000 genomes]
rs73245146	0.94[EUR][1000 genomes]
rs73245148	0.94[EUR][1000 genomes]
rs73245149	0.94[EUR][1000 genomes]
rs73245156	0.94[EUR][1000 genomes]
rs73245162	0.94[EUR][1000 genomes]
rs73245163	0.94[EUR][1000 genomes]
rs73245170	0.94[EUR][1000 genomes]
rs73245176	0.94[EUR][1000 genomes]
rs73245177	0.94[EUR][1000 genomes]
rs7442529	0.94[EUR][1000 genomes]
rs756299	0.94[EUR][1000 genomes]
rs756300	0.94[EUR][1000 genomes]
rs7657146	0.95[EUR][1000 genomes]
rs7663975	0.94[EUR][1000 genomes]
rs7664201	0.94[EUR][1000 genomes]
rs7664504	0.95[EUR][1000 genomes]
rs7665424	0.95[EUR][1000 genomes]
rs7674804	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7685953	0.94[EUR][1000 genomes]
rs7689383	0.95[EUR][1000 genomes]
rs7698682	0.94[EUR][1000 genomes]
rs7699158	0.94[EUR][1000 genomes]
rs868276	0.94[EUR][1000 genomes]
rs883314	0.95[EUR][1000 genomes]
rs884832	0.94[EUR][1000 genomes]
rs955784	0.97[EUR][1000 genomes]
rs955785	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs955786	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9684289	0.84[ASN][1000 genomes]
rs995843	0.94[EUR][1000 genomes]
rs9992463	0.95[EUR][1000 genomes]
rs9999625	0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817467	chr4:21602921-22422816	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv428756	chr4:22239826-22406106	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:22329000-22389400	Weak transcription	Pancreas	Pancrea
2	chr4:22336600-22385400	Weak transcription	Fetal Intestine Large	intestine
3	chr4:22354000-22378200	Weak transcription	Aorta	Aorta
4	chr4:22365600-22386800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:22365800-22384600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:22366000-22371400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr4:22366000-22385000	Weak transcription	NHEK	skin
8	chr4:22368800-22418600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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