Variant report

Variant	rs11768292
Chromosome Location	chr7:65474801-65474802
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:65470192..65472672-chr7:65474306..65476298,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 19 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10229450	0.86[ASN][1000 genomes]
rs10807697	0.81[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1167385	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1167386	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11763147	1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];0.85[TSI][hapmap]
rs11770828	0.87[CHB][hapmap]
rs12670952	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12698512	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1631091	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1701751	0.83[EUR][1000 genomes]
rs1701757	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1701760	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1723268	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1723275	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1829943	1.00[CHB][hapmap]
rs1880556	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1917563	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];0.86[JPT][hapmap];0.85[TSI][hapmap];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2008188	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2462573	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2658585	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2658587	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2692056	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2939548	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2946579	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2949690	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2949692	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3201569	0.89[ASN][1000 genomes]
rs34973832	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];0.86[JPT][hapmap];0.80[MEX][hapmap];0.85[TSI][hapmap];0.89[ASN][1000 genomes]
rs35135885	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35850374	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.86[JPT][hapmap];0.80[MEX][hapmap];0.87[TSI][hapmap];0.80[ASN][1000 genomes]
rs4467826	0.80[ASN][1000 genomes]
rs56028712	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs66552782	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6945322	0.81[ASN][1000 genomes]
rs6954920	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6955582	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6960048	0.81[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.88[ASN][1000 genomes]
rs6968534	1.00[ASW][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.94[MKK][hapmap]
rs709604	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs736270	1.00[CHB][hapmap];0.96[CHD][hapmap];0.91[GIH][hapmap];0.86[JPT][hapmap];0.85[TSI][hapmap];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7383796	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7784623	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.86[JPT][hapmap];0.80[MEX][hapmap];0.87[TSI][hapmap];0.88[ASN][1000 genomes]
rs7791814	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.86[JPT][hapmap];0.80[MEX][hapmap];0.85[TSI][hapmap]
rs7809991	0.89[ASN][1000 genomes]
rs781143	0.82[CEU][hapmap];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs781144	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs781145	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs781151	0.82[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.89[TSI][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs781152	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9530	0.82[CEU][hapmap];0.93[CHB][hapmap];0.81[CHD][hapmap];0.97[GIH][hapmap];0.86[JPT][hapmap];0.87[TSI][hapmap];0.83[EUR][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	esv2761079	chr7:65092426-65689733	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv532124	chr7:65371521-66234730	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	125 gene(s)	inside rSNPs	diseases
3	nsv1025494	chr7:65402301-65515606	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv538906	chr7:65402301-65515606	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:19)

SNP	Gene	Cis/trans	Tissue	Source
rs11768292	RP4-756H11.3	cis	Artery Tibial	GTEx
rs11768292	ZNF273	cis	cerebellum	SCAN
rs11768292	RP13-254B10.1	cis	Skin Sun Exposed Lower leg	GTEx
rs11768292	RP4-756H11.3	cis	Esophagus Muscularis	GTEx
rs11768292	ERV3	cis	parietal	SCAN
rs11768292	RP4-756H11.3	cis	Thyroid	GTEx
rs11768292	RP4-756H11.3	cis	Skin Sun Exposed Lower leg	GTEx
rs11768292	KCTD7	cis	parietal	SCAN
rs11768292	CRCP	cis	parietal	SCAN
rs11768292	RP4-756H11.3	cis	Adipose Subcutaneous	GTEx
rs11768292	RP4-756H11.3	cis	Nerve Tibial	GTEx
rs11768292	ERV3	cis	cerebellum	SCAN
rs11768292	GUSB	cis	parietal	SCAN
rs11768292	RABGEF1	cis	cerebellum	SCAN
rs11768292	GUSB	cis	cerebellum	SCAN
rs11768292	RP4-756H11.3	cis	lung	GTEx
rs11768292	RP4-756H11.3	cis	Esophagus Mucosa	GTEx
rs11768292	RP4-756H11.3	cis	Heart Left Ventricle	GTEx
rs11768292	CRCP	cis	cerebellum	SCAN

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65449200-65480400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:65472200-65478600	Weak transcription	Fetal Intestine Small	intestine
3	chr7:65474400-65477600	Weak transcription	HepG2	liver

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