Variant report

Variant	rs72637356
Chromosome Location	chr17:16511552-16511553
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 116 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:109)

rs_ID	r²[population]
rs1005369	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1005370	1.00[ASN][1000 genomes]
rs12051673	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12103873	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs16959857	1.00[ASN][1000 genomes]
rs16959869	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16959870	1.00[ASN][1000 genomes]
rs28398264	0.89[EUR][1000 genomes]
rs28431824	0.98[ASN][1000 genomes]
rs28458310	0.98[ASN][1000 genomes]
rs28458353	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28525101	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28525658	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28526077	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28612609	0.87[ASN][1000 genomes]
rs28626982	0.98[ASN][1000 genomes]
rs28636605	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28674185	0.98[ASN][1000 genomes]
rs28751872	0.98[ASN][1000 genomes]
rs28754336	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28792801	1.00[ASN][1000 genomes]
rs28826699	1.00[ASN][1000 genomes]
rs28865976	1.00[ASN][1000 genomes]
rs28875211	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3813762	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4239135	0.83[ASN][1000 genomes]
rs4352086	0.98[ASN][1000 genomes]
rs4791672	0.99[ASN][1000 genomes]
rs4791673	1.00[ASN][1000 genomes]
rs4791676	0.98[ASN][1000 genomes]
rs4791678	0.98[ASN][1000 genomes]
rs4792757	1.00[ASN][1000 genomes]
rs4792760	0.97[ASN][1000 genomes]
rs4792761	0.98[ASN][1000 genomes]
rs4792762	0.98[ASN][1000 genomes]
rs5000166	0.98[ASN][1000 genomes]
rs55920274	0.98[ASN][1000 genomes]
rs56303920	0.98[ASN][1000 genomes]
rs57448521	0.98[ASN][1000 genomes]
rs58164310	0.98[ASN][1000 genomes]
rs59486407	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59594997	0.98[ASN][1000 genomes]
rs59826203	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62072781	1.00[ASN][1000 genomes]
rs62072790	0.87[ASN][1000 genomes]
rs62072792	1.00[ASN][1000 genomes]
rs62072845	0.96[ASN][1000 genomes]
rs62073660	1.00[ASN][1000 genomes]
rs6502514	1.00[ASN][1000 genomes]
rs7208075	0.98[ASN][1000 genomes]
rs7213274	0.98[ASN][1000 genomes]
rs7217544	1.00[ASN][1000 genomes]
rs7217717	1.00[ASN][1000 genomes]
rs7218241	0.98[ASN][1000 genomes]
rs7219632	1.00[ASN][1000 genomes]
rs7221518	0.98[ASN][1000 genomes]
rs7222622	0.84[ASN][1000 genomes]
rs7222875	0.98[ASN][1000 genomes]
rs7225641	0.98[ASN][1000 genomes]
rs7226328	0.82[ASN][1000 genomes]
rs72637355	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72637357	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72637358	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72637359	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72637360	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72637361	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72637362	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72637363	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8065558	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8068349	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8069286	0.80[ASN][1000 genomes]
rs8074285	1.00[ASN][1000 genomes]
rs8074464	1.00[ASN][1000 genomes]
rs8074487	0.98[ASN][1000 genomes]
rs8075988	1.00[ASN][1000 genomes]
rs8076849	0.98[ASN][1000 genomes]
rs8082225	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8082650	0.98[ASN][1000 genomes]
rs9889227	1.00[ASN][1000 genomes]
rs9890123	1.00[ASN][1000 genomes]
rs9890698	1.00[ASN][1000 genomes]
rs9891138	1.00[ASN][1000 genomes]
rs9894637	1.00[ASN][1000 genomes]
rs9898888	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9899785	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9899919	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9901145	0.87[ASN][1000 genomes]
rs9904901	1.00[ASN][1000 genomes]
rs9905710	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9906261	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9906728	1.00[ASN][1000 genomes]
rs9907785	1.00[ASN][1000 genomes]
rs9908015	0.98[ASN][1000 genomes]
rs9908390	0.98[ASN][1000 genomes]
rs9909044	1.00[ASN][1000 genomes]
rs9909955	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9910087	1.00[ASN][1000 genomes]
rs9910842	0.98[ASN][1000 genomes]
rs9911162	0.98[ASN][1000 genomes]
rs9911524	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9911608	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9911677	0.83[ASN][1000 genomes]
rs9911820	0.98[ASN][1000 genomes]
rs9911851	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9915121	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9916069	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9916258	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9916464	0.89[EUR][1000 genomes]
rs9916819	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934185	chr17:15552960-16551197	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	190 gene(s)	inside rSNPs	diseases
2	esv3330182	chr17:15652014-16569534	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
3	esv3446844	chr17:15654843-16572246	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
4	nsv1063459	chr17:15804228-16543593	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
5	nsv1063764	chr17:16171649-16662914	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	120 gene(s)	inside rSNPs	diseases
6	nsv1058448	chr17:16389870-16926287	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
7	nsv962267	chr17:16511230-16520679	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16505000-16511600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr17:16509000-16511800	Weak transcription	Brain Substantia Nigra	brain
3	chr17:16510000-16518200	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr17:16511200-16513600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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