Variant report

Variant	rs72637361
Chromosome Location	chr17:16577159-16577160
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 113 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs1005369	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1005370	0.85[ASN][1000 genomes]
rs12051673	0.83[ASN][1000 genomes]
rs12103873	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16959857	0.85[ASN][1000 genomes]
rs16959869	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16959870	0.85[ASN][1000 genomes]
rs28398264	0.88[EUR][1000 genomes]
rs28431824	0.85[ASN][1000 genomes]
rs28458310	0.85[ASN][1000 genomes]
rs28458353	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28525101	0.88[EUR][1000 genomes]
rs28525658	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28526077	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28612609	0.97[ASN][1000 genomes]
rs28626982	0.85[ASN][1000 genomes]
rs28636605	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28674185	0.85[ASN][1000 genomes]
rs28751872	0.85[ASN][1000 genomes]
rs28754336	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28792801	0.85[ASN][1000 genomes]
rs28826699	0.85[ASN][1000 genomes]
rs28865976	0.85[ASN][1000 genomes]
rs28875211	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3813762	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4352086	0.85[ASN][1000 genomes]
rs4791672	0.85[ASN][1000 genomes]
rs4791673	0.85[ASN][1000 genomes]
rs4791676	0.85[ASN][1000 genomes]
rs4791678	0.85[ASN][1000 genomes]
rs4792757	0.85[ASN][1000 genomes]
rs4792760	0.87[ASN][1000 genomes]
rs4792761	0.85[ASN][1000 genomes]
rs4792762	0.85[ASN][1000 genomes]
rs5000166	0.85[ASN][1000 genomes]
rs55920274	0.83[ASN][1000 genomes]
rs56303920	0.85[ASN][1000 genomes]
rs57448521	0.83[ASN][1000 genomes]
rs58164310	0.85[ASN][1000 genomes]
rs59486407	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs59594997	0.85[ASN][1000 genomes]
rs59826203	0.85[ASN][1000 genomes]
rs62072781	0.85[ASN][1000 genomes]
rs62072792	0.85[ASN][1000 genomes]
rs62072845	0.82[ASN][1000 genomes]
rs62073660	0.85[ASN][1000 genomes]
rs6502514	0.85[ASN][1000 genomes]
rs7208075	0.85[ASN][1000 genomes]
rs7213274	0.85[ASN][1000 genomes]
rs7217544	0.85[ASN][1000 genomes]
rs7217717	0.85[ASN][1000 genomes]
rs7218241	0.85[ASN][1000 genomes]
rs7219632	0.85[ASN][1000 genomes]
rs7221518	0.85[ASN][1000 genomes]
rs7222875	0.85[ASN][1000 genomes]
rs7225641	0.85[ASN][1000 genomes]
rs72637355	0.82[ASN][1000 genomes]
rs72637356	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72637357	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72637358	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72637359	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72637360	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72637362	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72637363	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8065558	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8068349	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8074285	0.85[ASN][1000 genomes]
rs8074464	0.85[ASN][1000 genomes]
rs8074487	0.85[ASN][1000 genomes]
rs8075988	0.85[ASN][1000 genomes]
rs8076849	0.85[ASN][1000 genomes]
rs8082225	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8082650	0.85[ASN][1000 genomes]
rs9889227	0.85[ASN][1000 genomes]
rs9890123	0.85[ASN][1000 genomes]
rs9890698	0.85[ASN][1000 genomes]
rs9891138	0.85[ASN][1000 genomes]
rs9894637	0.85[ASN][1000 genomes]
rs9898888	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9899785	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9899919	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9904901	0.85[ASN][1000 genomes]
rs9905710	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9906261	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9906728	0.85[ASN][1000 genomes]
rs9907785	0.85[ASN][1000 genomes]
rs9908015	0.85[ASN][1000 genomes]
rs9908390	0.85[ASN][1000 genomes]
rs9909044	0.85[ASN][1000 genomes]
rs9909955	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9910087	0.85[ASN][1000 genomes]
rs9910842	0.85[ASN][1000 genomes]
rs9911162	0.85[ASN][1000 genomes]
rs9911524	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9911608	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9911820	0.85[ASN][1000 genomes]
rs9911851	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9915121	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9916069	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9916258	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9916464	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	esv2758442	chr17:16527056-16817437	Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	esv2758676	chr17:16527056-16817437	Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
5	nsv427991	chr17:16527056-16817437	Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
6	nsv907720	chr17:16557606-16758204	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
7	nsv978372	chr17:16559570-16587380	Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	esv2756642	chr17:16571504-16734163	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
9	esv2757653	chr17:16571504-16764830	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
10	nsv984504	chr17:16572370-16776542	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
11	esv3315162	chr17:16573497-16587377	Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
12	esv3315164	chr17:16573497-16587377	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16571000-16579600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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