Variant report

Variant	rs7426713
Chromosome Location	chr3:162443292-162443293
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 117 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:103)

rs_ID	r²[population]
rs10936308	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11922500	0.85[EUR][1000 genomes]
rs11923566	0.80[AMR][1000 genomes]
rs11925750	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11926645	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12489679	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12496550	0.88[ASN][1000 genomes]
rs12496594	0.81[ASN][1000 genomes]
rs12496614	0.93[ASN][1000 genomes]
rs12631404	0.85[ASN][1000 genomes]
rs12635779	0.85[ASN][1000 genomes]
rs13063582	0.80[AMR][1000 genomes]
rs13069139	0.80[AMR][1000 genomes]
rs13077716	0.80[AMR][1000 genomes]
rs13083886	0.84[EUR][1000 genomes]
rs13085871	0.80[AMR][1000 genomes]
rs13092433	0.80[AMR][1000 genomes]
rs13092614	0.80[AMR][1000 genomes]
rs13092643	0.80[AMR][1000 genomes]
rs13093719	0.88[ASN][1000 genomes]
rs1353556	0.93[ASN][1000 genomes]
rs1353557	0.93[ASN][1000 genomes]
rs1353558	0.80[AMR][1000 genomes]
rs1566063	0.80[AMR][1000 genomes]
rs16851335	0.81[ASN][1000 genomes]
rs1874510	0.82[EUR][1000 genomes]
rs1874512	0.82[EUR][1000 genomes]
rs2029925	0.85[EUR][1000 genomes]
rs2173065	0.80[AMR][1000 genomes]
rs2173066	0.80[AMR][1000 genomes]
rs2173067	0.80[AMR][1000 genomes]
rs2361609	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4858909	0.80[AMR][1000 genomes]
rs4858911	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs55807361	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56162745	0.85[ASN][1000 genomes]
rs56242739	0.86[EUR][1000 genomes]
rs56815734	0.85[ASN][1000 genomes]
rs57617609	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58194889	0.89[ASN][1000 genomes]
rs58604878	0.85[ASN][1000 genomes]
rs59027724	0.88[ASN][1000 genomes]
rs59307821	0.85[ASN][1000 genomes]
rs61170375	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62292528	0.80[AMR][1000 genomes]
rs62292532	0.80[AMR][1000 genomes]
rs62294571	0.80[AMR][1000 genomes]
rs62294573	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62294579	0.81[ASN][1000 genomes]
rs62294581	0.91[ASN][1000 genomes]
rs6414405	0.81[AMR][1000 genomes]
rs6414407	0.86[EUR][1000 genomes]
rs6441540	0.84[EUR][1000 genomes]
rs6441541	0.84[EUR][1000 genomes]
rs6441542	0.80[AMR][1000 genomes]
rs6441543	0.85[EUR][1000 genomes]
rs6441545	0.86[EUR][1000 genomes]
rs6441546	0.94[ASN][1000 genomes]
rs6764576	0.86[EUR][1000 genomes]
rs6778765	0.85[EUR][1000 genomes]
rs6798611	0.83[AMR][1000 genomes]
rs73010393	0.85[ASN][1000 genomes]
rs73010394	0.85[ASN][1000 genomes]
rs73010402	0.85[ASN][1000 genomes]
rs73876101	0.85[ASN][1000 genomes]
rs7427964	0.85[EUR][1000 genomes]
rs7427978	0.85[EUR][1000 genomes]
rs7429617	0.82[AMR][1000 genomes]
rs7429718	0.82[AMR][1000 genomes]
rs7431330	0.82[AMR][1000 genomes]
rs7431666	0.80[AMR][1000 genomes]
rs7433034	0.80[AMR][1000 genomes]
rs7433394	0.80[AMR][1000 genomes]
rs7433902	0.85[EUR][1000 genomes]
rs7615986	0.80[AMR][1000 genomes]
rs7628666	0.80[AMR][1000 genomes]
rs7630042	0.85[EUR][1000 genomes]
rs7633892	0.85[ASN][1000 genomes]
rs7634217	0.85[EUR][1000 genomes]
rs7640151	0.83[ASN][1000 genomes]
rs7646046	0.85[EUR][1000 genomes]
rs7652225	0.85[ASN][1000 genomes]
rs7652373	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7652432	0.85[EUR][1000 genomes]
rs903942	0.80[AMR][1000 genomes]
rs9810012	0.85[EUR][1000 genomes]
rs9813079	0.82[EUR][1000 genomes]
rs9815680	0.83[AMR][1000 genomes]
rs9816330	0.82[AMR][1000 genomes]
rs9823808	0.80[AMR][1000 genomes]
rs9831314	0.85[EUR][1000 genomes]
rs9832503	0.85[EUR][1000 genomes]
rs9839936	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9840341	0.80[AMR][1000 genomes]
rs9844124	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9859307	0.84[EUR][1000 genomes]
rs9867696	0.93[ASN][1000 genomes]
rs9870314	0.85[EUR][1000 genomes]
rs9874108	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9878965	0.83[EUR][1000 genomes]
rs9882410	0.82[EUR][1000 genomes]
rs9882755	0.82[EUR][1000 genomes]
rs9883543	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006802	chr3:161921063-162599175	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv428424	chr3:162145988-163033943	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1012160	chr3:162182166-162540478	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv592201	chr3:162188625-163142162	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv470994	chr3:162217993-162945834	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv1005142	chr3:162284967-162447818	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv877758	chr3:162287573-162521339	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv877759	chr3:162303276-162521339	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv877761	chr3:162346392-162521339	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv1005637	chr3:162379324-162635451	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv877762	chr3:162400620-162521339	Enhancers Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
12	nsv869804	chr3:162414099-162776884	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv829776	chr3:162422424-162577578	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
14	nsv1001282	chr3:162429561-162513137	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:162439800-162459200	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr3:162441200-162447000	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr3:162441800-162446400	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr3:162441800-162446600	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr3:162442200-162445200	Weak transcription	Dnd41	blood
6	chr3:162442200-162445800	Active TSS	HUES64 Cell Line	embryonic stem cell
7	chr3:162442200-162447200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr3:162442600-162445000	Active TSS	H9 Cell Line	embryonic stem cell
9	chr3:162442600-162445600	Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr3:162442800-162444200	Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr3:162443000-162443800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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