Variant report

Variant	rs12520161
Chromosome Location	chr5:119494492-119494493
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 125 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:116)

rs_ID	r²[population]
rs10043143	0.84[ASN][1000 genomes]
rs10052192	0.84[ASN][1000 genomes]
rs10052564	0.89[ASN][1000 genomes]
rs10053118	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10066059	0.88[ASN][1000 genomes]
rs10079429	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1031130	0.95[ASN][1000 genomes]
rs1031131	0.95[ASN][1000 genomes]
rs10900735	0.92[ASN][1000 genomes]
rs11951475	0.89[ASN][1000 genomes]
rs11951498	0.88[ASN][1000 genomes]
rs12517429	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12520785	0.91[ASN][1000 genomes]
rs12520817	0.91[ASN][1000 genomes]
rs12521813	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12522508	0.89[ASN][1000 genomes]
rs12522857	0.83[ASN][1000 genomes]
rs12523293	0.88[ASN][1000 genomes]
rs13183113	0.98[ASN][1000 genomes]
rs1348474	0.99[ASN][1000 genomes]
rs1348478	0.89[ASN][1000 genomes]
rs1348479	0.89[ASN][1000 genomes]
rs1373317	0.99[ASN][1000 genomes]
rs1373318	0.99[ASN][1000 genomes]
rs1373320	0.91[ASN][1000 genomes]
rs1373324	0.89[ASN][1000 genomes]
rs1443966	0.99[ASN][1000 genomes]
rs1443969	0.95[ASN][1000 genomes]
rs1443970	0.92[ASN][1000 genomes]
rs1443980	0.89[ASN][1000 genomes]
rs1443981	0.88[ASN][1000 genomes]
rs1443985	0.89[ASN][1000 genomes]
rs1443986	0.89[ASN][1000 genomes]
rs1443987	0.89[ASN][1000 genomes]
rs1470349	0.87[ASN][1000 genomes]
rs1470350	0.85[ASN][1000 genomes]
rs17146058	0.89[ASN][1000 genomes]
rs17146063	0.83[ASN][1000 genomes]
rs17146068	0.89[ASN][1000 genomes]
rs17146098	0.87[ASN][1000 genomes]
rs17146149	0.92[ASN][1000 genomes]
rs17146179	0.95[ASN][1000 genomes]
rs17146184	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1862306	0.95[ASN][1000 genomes]
rs1862307	0.95[ASN][1000 genomes]
rs1907193	0.89[ASN][1000 genomes]
rs1907194	0.89[ASN][1000 genomes]
rs1974787	0.81[ASN][1000 genomes]
rs1981819	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2053622	0.89[ASN][1000 genomes]
rs2059093	0.87[ASN][1000 genomes]
rs2130738	0.89[ASN][1000 genomes]
rs2130739	0.89[ASN][1000 genomes]
rs2161303	0.95[ASN][1000 genomes]
rs2166013	0.88[ASN][1000 genomes]
rs28635608	0.90[ASN][1000 genomes]
rs2897117	0.91[ASN][1000 genomes]
rs34287269	0.81[ASN][1000 genomes]
rs35236191	0.86[ASN][1000 genomes]
rs35463506	0.92[ASN][1000 genomes]
rs35648087	0.90[ASN][1000 genomes]
rs35758661	0.89[ASN][1000 genomes]
rs3991623	0.83[ASN][1000 genomes]
rs41447148	0.92[ASN][1000 genomes]
rs4446498	0.90[ASN][1000 genomes]
rs4446499	0.91[ASN][1000 genomes]
rs4868423	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55635066	0.89[ASN][1000 genomes]
rs56151766	0.89[ASN][1000 genomes]
rs56186068	0.89[ASN][1000 genomes]
rs56352443	0.91[ASN][1000 genomes]
rs57510292	0.95[ASN][1000 genomes]
rs58036644	0.84[ASN][1000 genomes]
rs59845464	0.95[ASN][1000 genomes]
rs60408531	0.92[ASN][1000 genomes]
rs60547170	0.90[ASN][1000 genomes]
rs60772350	0.95[ASN][1000 genomes]
rs61395607	0.94[ASN][1000 genomes]
rs62376993	0.91[ASN][1000 genomes]
rs62376998	0.95[ASN][1000 genomes]
rs62377003	0.87[ASN][1000 genomes]
rs62377004	0.81[ASN][1000 genomes]
rs62377005	0.99[ASN][1000 genomes]
rs6595211	0.95[ASN][1000 genomes]
rs6866827	0.92[ASN][1000 genomes]
rs6868570	0.97[ASN][1000 genomes]
rs6868780	0.89[ASN][1000 genomes]
rs6873570	0.91[ASN][1000 genomes]
rs6874351	0.88[ASN][1000 genomes]
rs6874504	0.88[ASN][1000 genomes]
rs6877170	0.92[ASN][1000 genomes]
rs6879182	0.95[ASN][1000 genomes]
rs6882395	0.92[ASN][1000 genomes]
rs6883507	0.92[ASN][1000 genomes]
rs6888177	0.89[ASN][1000 genomes]
rs6888446	0.89[ASN][1000 genomes]
rs6889996	0.91[ASN][1000 genomes]
rs6895104	0.85[ASN][1000 genomes]
rs6898633	0.88[ASN][1000 genomes]
rs718734	0.84[ASN][1000 genomes]
rs718735	0.84[ASN][1000 genomes]
rs719191	0.95[ASN][1000 genomes]
rs73266681	0.95[ASN][1000 genomes]
rs7702005	0.89[ASN][1000 genomes]
rs7705480	0.89[ASN][1000 genomes]
rs7707700	0.91[ASN][1000 genomes]
rs7722633	0.89[ASN][1000 genomes]
rs7730558	0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9327125	0.89[ASN][1000 genomes]
rs9327129	0.91[ASN][1000 genomes]
rs953189	0.87[ASN][1000 genomes]
rs982358	0.95[ASN][1000 genomes]
rs982605	0.95[ASN][1000 genomes]
rs982606	0.95[ASN][1000 genomes]
rs982607	0.95[ASN][1000 genomes]
rs994630	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023146	chr5:119301891-119623417	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv537883	chr5:119301891-119623417	Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv3331559	chr5:119306944-119536554	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv532200	chr5:119317901-120102513	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv882781	chr5:119369334-119557828	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv599600	chr5:119399177-119507243	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv432803	chr5:119419101-119659101	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv1016024	chr5:119460796-119509057	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
9	nsv1018247	chr5:119469805-119511846	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:119488600-119495800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:119492200-119495200	Weak transcription	Hela-S3	cervix

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