Variant report

Variant	rs13421353
Chromosome Location	chr2:101147087-101147088
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 98 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs10166130	0.82[EUR][1000 genomes]
rs10166865	0.80[EUR][1000 genomes]
rs10175632	0.89[CHB][hapmap]
rs10180172	0.85[CHB][hapmap]
rs10183360	0.86[EUR][1000 genomes]
rs10195487	0.86[EUR][1000 genomes]
rs10195943	0.90[CHB][hapmap]
rs10210508	0.82[CHB][hapmap]
rs10865040	0.86[EUR][1000 genomes]
rs11884976	0.90[CHB][hapmap]
rs11891670	0.81[CHB][hapmap]
rs11892956	0.80[EUR][1000 genomes]
rs11898188	0.82[CEU][hapmap];0.89[CHB][hapmap]
rs11902961	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12233152	0.93[ASN][1000 genomes]
rs12464855	0.81[CHB][hapmap]
rs12465627	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12466753	0.82[EUR][1000 genomes]
rs12469068	0.86[EUR][1000 genomes]
rs12475281	0.82[EUR][1000 genomes]
rs12475282	0.82[EUR][1000 genomes]
rs13383447	0.84[EUR][1000 genomes]
rs13385681	0.80[EUR][1000 genomes]
rs13388529	0.80[EUR][1000 genomes]
rs13389527	0.80[EUR][1000 genomes]
rs13399092	0.86[EUR][1000 genomes]
rs13408862	0.94[CEU][hapmap];0.85[CHB][hapmap];0.86[EUR][1000 genomes]
rs13411940	0.80[EUR][1000 genomes]
rs13412463	0.86[EUR][1000 genomes]
rs13414632	0.80[EUR][1000 genomes]
rs13414838	0.80[EUR][1000 genomes]
rs13415591	0.90[CHB][hapmap]
rs13419419	0.89[ASN][1000 genomes]
rs13430695	0.80[EUR][1000 genomes]
rs1437968	0.89[CHB][hapmap]
rs1437974	0.90[CHB][hapmap]
rs1519656	0.83[EUR][1000 genomes]
rs1519657	0.83[EUR][1000 genomes]
rs17024335	0.80[EUR][1000 genomes]
rs17024441	0.82[EUR][1000 genomes]
rs17024477	0.95[ASN][1000 genomes]
rs17024489	0.91[ASN][1000 genomes]
rs2309861	0.94[CEU][hapmap];0.90[CHB][hapmap];0.86[EUR][1000 genomes]
rs2309863	0.89[CHB][hapmap]
rs2871350	0.88[ASN][1000 genomes]
rs4147028	0.91[ASN][1000 genomes]
rs4368352	0.82[EUR][1000 genomes]
rs4581914	0.80[EUR][1000 genomes]
rs4589783	0.85[EUR][1000 genomes]
rs4630791	0.80[EUR][1000 genomes]
rs4632365	0.80[EUR][1000 genomes]
rs4633941	0.80[EUR][1000 genomes]
rs56304912	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs57819301	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs60453957	0.86[EUR][1000 genomes]
rs62155208	0.88[EUR][1000 genomes]
rs6542954	0.86[EUR][1000 genomes]
rs6542955	0.80[EUR][1000 genomes]
rs6542956	0.86[EUR][1000 genomes]
rs6542960	0.80[EUR][1000 genomes]
rs6542962	0.82[EUR][1000 genomes]
rs6542963	0.87[EUR][1000 genomes]
rs6542965	0.90[CHB][hapmap];0.86[EUR][1000 genomes]
rs6542966	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6718127	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6722896	0.90[CHB][hapmap];0.86[EUR][1000 genomes]
rs6731045	0.86[EUR][1000 genomes]
rs6735337	0.80[EUR][1000 genomes]
rs6739721	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6747630	0.84[EUR][1000 genomes]
rs6755846	0.87[CEU][hapmap];0.89[CHB][hapmap];0.86[EUR][1000 genomes]
rs6760452	0.80[EUR][1000 genomes]
rs750033	0.80[EUR][1000 genomes]
rs7561811	0.80[EUR][1000 genomes]
rs7565675	0.80[EUR][1000 genomes]
rs7568283	0.80[EUR][1000 genomes]
rs7568519	0.80[EUR][1000 genomes]
rs7576144	0.86[EUR][1000 genomes]
rs7578352	0.80[EUR][1000 genomes]
rs7592840	0.80[EUR][1000 genomes]
rs7593928	0.86[EUR][1000 genomes]
rs7595834	0.87[ASN][1000 genomes]
rs7596851	0.80[EUR][1000 genomes]
rs7597254	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7598078	0.90[EUR][1000 genomes]
rs7598339	0.90[EUR][1000 genomes]
rs7599321	0.80[EUR][1000 genomes]
rs7602968	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7606473	0.86[EUR][1000 genomes]
rs9308837	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9653443	0.90[CHB][hapmap]
rs9917224	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007777	chr2:100816913-101308914	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
2	nsv535844	chr2:100816913-101308914	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	nsv582531	chr2:100908508-101207639	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv916792	chr2:101021066-101525200	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	nsv582532	chr2:101029002-101531943	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv834312	chr2:101044438-101238166	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 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	chr2:101136800-101149000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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