Variant report

Variant	rs1003909
Chromosome Location	chr4:95756446-95756447
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 105 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs10003866	0.92[ASN][1000 genomes]
rs10003992	0.87[ASN][1000 genomes]
rs10004286	0.97[ASN][1000 genomes]
rs10004478	0.92[ASN][1000 genomes]
rs10004573	0.92[ASN][1000 genomes]
rs10005096	0.90[ASN][1000 genomes]
rs10005252	0.90[ASN][1000 genomes]
rs10005450	0.90[ASN][1000 genomes]
rs10010959	0.92[ASN][1000 genomes]
rs10014945	0.92[ASN][1000 genomes]
rs10015222	0.92[ASN][1000 genomes]
rs10017163	0.83[ASN][1000 genomes]
rs10017575	0.92[ASN][1000 genomes]
rs10027656	0.90[ASN][1000 genomes]
rs10033559	0.90[ASN][1000 genomes]
rs10212893	0.91[ASN][1000 genomes]
rs11097441	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11097443	0.92[ASN][1000 genomes]
rs11097444	0.92[ASN][1000 genomes]
rs11097445	0.92[ASN][1000 genomes]
rs11934778	0.96[ASN][1000 genomes]
rs11946778	0.99[ASN][1000 genomes]
rs12500280	0.95[ASN][1000 genomes]
rs12500330	0.95[ASN][1000 genomes]
rs13103529	0.92[ASN][1000 genomes]
rs13117041	0.90[ASN][1000 genomes]
rs13117507	0.90[ASN][1000 genomes]
rs13127197	0.91[ASN][1000 genomes]
rs13127435	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13127833	0.92[ASN][1000 genomes]
rs13127842	0.92[ASN][1000 genomes]
rs13127888	0.92[ASN][1000 genomes]
rs13139046	0.99[ASN][1000 genomes]
rs13149762	0.90[ASN][1000 genomes]
rs13150342	0.90[ASN][1000 genomes]
rs13151193	0.92[ASN][1000 genomes]
rs1319314	0.89[ASN][1000 genomes]
rs1319315	0.89[ASN][1000 genomes]
rs1319316	0.89[ASN][1000 genomes]
rs1544386	0.90[ASN][1000 genomes]
rs1544387	0.90[ASN][1000 genomes]
rs1544388	0.88[ASN][1000 genomes]
rs1544389	0.88[ASN][1000 genomes]
rs1544390	0.85[ASN][1000 genomes]
rs1544391	0.87[ASN][1000 genomes]
rs1544392	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1544393	0.89[ASN][1000 genomes]
rs2865413	0.90[ASN][1000 genomes]
rs4254781	0.89[ASN][1000 genomes]
rs4256228	0.89[ASN][1000 genomes]
rs4361394	0.88[ASN][1000 genomes]
rs4364269	0.89[ASN][1000 genomes]
rs4429734	0.89[ASN][1000 genomes]
rs4437261	0.88[ASN][1000 genomes]
rs4538488	0.89[ASN][1000 genomes]
rs6532511	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6532512	0.92[ASN][1000 genomes]
rs6812504	0.92[ASN][1000 genomes]
rs6816019	0.96[ASN][1000 genomes]
rs6816482	0.96[ASN][1000 genomes]
rs6817080	0.96[ASN][1000 genomes]
rs6817662	0.92[ASN][1000 genomes]
rs6828291	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6828354	0.90[ASN][1000 genomes]
rs6828538	0.90[ASN][1000 genomes]
rs6828821	0.90[ASN][1000 genomes]
rs6828950	0.90[ASN][1000 genomes]
rs6829477	0.89[ASN][1000 genomes]
rs6831418	0.97[ASN][1000 genomes]
rs6834911	0.94[ASN][1000 genomes]
rs6835688	0.92[ASN][1000 genomes]
rs6843053	0.92[ASN][1000 genomes]
rs6847607	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6848017	0.88[ASN][1000 genomes]
rs6851643	0.89[ASN][1000 genomes]
rs6851987	0.92[ASN][1000 genomes]
rs6854743	0.90[ASN][1000 genomes]
rs6857888	0.96[ASN][1000 genomes]
rs6858126	0.94[ASN][1000 genomes]
rs6858132	0.94[ASN][1000 genomes]
rs6858143	0.94[ASN][1000 genomes]
rs6858333	0.96[ASN][1000 genomes]
rs6858439	0.96[ASN][1000 genomes]
rs6858699	0.96[ASN][1000 genomes]
rs7654266	0.89[ASN][1000 genomes]
rs7663201	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7663374	0.99[ASN][1000 genomes]
rs7676033	0.89[ASN][1000 genomes]
rs7691832	0.92[ASN][1000 genomes]
rs7692197	0.92[ASN][1000 genomes]
rs916876	0.89[ASN][1000 genomes]
rs916877	0.89[ASN][1000 genomes]
rs916878	0.89[ASN][1000 genomes]
rs9307148	0.90[ASN][1000 genomes]
rs978122	0.89[ASN][1000 genomes]
rs9992130	0.92[ASN][1000 genomes]
rs9995378	0.92[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	nsv932216	chr4:95501261-96109807	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1003860	chr4:95507683-96120619	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv869528	chr4:95537649-96368018	Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1005816	chr4:95573444-95902704	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv1007391	chr4:95713679-95763860	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv999588	chr4:95717063-95763860	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv997960	chr4:95719585-95766067	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv537188	chr4:95719585-95766067	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95750800-95764400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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