Variant report

Variant	rs7167366
Chromosome Location	chr15:39906377-39906378
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 127 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:119)

rs_ID	r²[population]
rs10152640	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10520137	0.96[ASN][1000 genomes]
rs10520138	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11070220	0.91[ASN][1000 genomes]
rs11070221	0.94[ASN][1000 genomes]
rs11070222	0.94[ASN][1000 genomes]
rs11070223	0.94[ASN][1000 genomes]
rs11070224	0.94[ASN][1000 genomes]
rs11070225	0.96[ASN][1000 genomes]
rs11070226	0.82[ASN][1000 genomes]
rs11070227	0.82[ASN][1000 genomes]
rs11070228	0.82[ASN][1000 genomes]
rs1134485	0.85[ASN][1000 genomes]
rs1134486	0.91[ASN][1000 genomes]
rs11630406	0.81[ASN][1000 genomes]
rs11631820	0.87[EUR][1000 genomes]
rs11631824	0.87[EUR][1000 genomes]
rs11632879	0.82[ASN][1000 genomes]
rs11635103	0.81[ASN][1000 genomes]
rs11638041	0.82[ASN][1000 genomes]
rs11638558	0.82[ASN][1000 genomes]
rs11852591	0.82[ASN][1000 genomes]
rs11852649	0.82[ASN][1000 genomes]
rs11855487	0.82[ASN][1000 genomes]
rs11856971	0.82[ASN][1000 genomes]
rs11857819	0.95[ASN][1000 genomes]
rs12050804	0.86[EUR][1000 genomes]
rs12443011	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12900583	0.84[EUR][1000 genomes]
rs12908846	0.96[ASN][1000 genomes]
rs12912082	0.86[ASN][1000 genomes]
rs1478604	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1478605	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs16969386	0.96[ASN][1000 genomes]
rs16969395	0.91[ASN][1000 genomes]
rs16969410	0.95[ASN][1000 genomes]
rs16969426	0.82[ASN][1000 genomes]
rs16969429	0.82[ASN][1000 genomes]
rs16969451	0.82[ASN][1000 genomes]
rs16969459	0.82[ASN][1000 genomes]
rs16969475	0.81[ASN][1000 genomes]
rs16969478	0.81[ASN][1000 genomes]
rs1876852	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1876853	0.82[ASN][1000 genomes]
rs1904209	0.84[ASN][1000 genomes]
rs2169830	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2228261	0.91[ASN][1000 genomes]
rs2229364	0.91[ASN][1000 genomes]
rs2292305	0.83[ASN][1000 genomes]
rs2411310	0.87[EUR][1000 genomes]
rs2411314	0.80[ASN][1000 genomes]
rs2411315	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2412412	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2412413	0.82[ASN][1000 genomes]
rs2412414	0.82[ASN][1000 genomes]
rs2412415	0.81[ASN][1000 genomes]
rs2412416	0.82[ASN][1000 genomes]
rs2412417	0.82[ASN][1000 genomes]
rs2412418	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2412419	0.93[ASN][1000 genomes]
rs2412420	0.94[ASN][1000 genomes]
rs2412421	0.88[ASN][1000 genomes]
rs2618162	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2618163	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2664139	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2664141	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2898688	0.82[ASN][1000 genomes]
rs2898962	0.82[ASN][1000 genomes]
rs3743125	0.91[ASN][1000 genomes]
rs4319738	0.87[EUR][1000 genomes]
rs4319740	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4349120	0.82[ASN][1000 genomes]
rs4429263	0.80[EUR][1000 genomes]
rs4479205	0.82[ASN][1000 genomes]
rs4493017	0.86[EUR][1000 genomes]
rs4505280	0.86[EUR][1000 genomes]
rs4526992	0.80[ASN][1000 genomes]
rs4547308	0.82[ASN][1000 genomes]
rs4628934	0.82[ASN][1000 genomes]
rs56938133	0.94[ASN][1000 genomes]
rs60164392	0.82[ASN][1000 genomes]
rs60195210	0.82[ASN][1000 genomes]
rs61130460	0.81[ASN][1000 genomes]
rs61568256	0.81[ASN][1000 genomes]
rs66781090	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs67239630	0.94[ASN][1000 genomes]
rs7162070	0.82[ASN][1000 genomes]
rs7162781	0.80[ASN][1000 genomes]
rs7167184	0.82[ASN][1000 genomes]
rs7168755	0.83[ASN][1000 genomes]
rs7169478	0.82[ASN][1000 genomes]
rs7169574	0.88[ASN][1000 genomes]
rs7170682	0.88[ASN][1000 genomes]
rs7176721	0.83[AMR][1000 genomes]
rs7177324	0.96[ASN][1000 genomes]
rs7179293	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7179608	0.80[ASN][1000 genomes]
rs7183544	0.87[ASN][1000 genomes]
rs72725079	0.82[ASN][1000 genomes]
rs72725080	0.82[ASN][1000 genomes]
rs72725084	0.82[ASN][1000 genomes]
rs753598	0.81[ASN][1000 genomes]
rs753599	0.85[ASN][1000 genomes]
rs8026916	0.82[ASN][1000 genomes]
rs8029602	0.81[ASN][1000 genomes]
rs8032035	0.96[ASN][1000 genomes]
rs8032289	0.82[ASN][1000 genomes]
rs8034594	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8035354	0.82[EUR][1000 genomes]
rs8036376	0.87[ASN][1000 genomes]
rs8036633	0.87[ASN][1000 genomes]
rs8039035	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9302102	0.89[ASN][1000 genomes]
rs949646	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs964424	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs970280	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9806365	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9806647	0.96[ASN][1000 genomes]
rs999393	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049682	chr15:39657279-40027403	Enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv542361	chr15:39657279-40027403	Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	esv3373125	chr15:39691567-40061262	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv904094	chr15:39738006-39976057	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv832977	chr15:39817512-39981520	Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
6	nsv1048628	chr15:39877498-39940104	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv1502	chr15:39884314-39928968	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
8	nsv832978	chr15:39899759-40094881	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:39904000-39913400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr15:39905000-39908400	Weak transcription	HUVEC	blood vessel
3	chr15:39905400-39906400	Enhancers	NHEK	skin
4	chr15:39905800-39906400	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr15:39905800-39906400	Enhancers	HMEC	breast
6	chr15:39906200-39908800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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