Variant report

Variant	rs10001065
Chromosome Location	chr4:69781318-69781319
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 106 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:95)

rs_ID	r²[population]
rs10000598	0.89[EUR][1000 genomes]
rs10000974	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10004381	0.86[AFR][1000 genomes]
rs10006282	0.89[EUR][1000 genomes]
rs10010699	0.89[EUR][1000 genomes]
rs10013724	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10014997	0.81[AFR][1000 genomes]
rs10024664	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10032748	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1020767	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1020768	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10518057	0.89[EUR][1000 genomes]
rs10903220	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10903221	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10903224	0.89[EUR][1000 genomes]
rs1117530	0.80[AFR][1000 genomes]
rs1117531	0.80[AFR][1000 genomes]
rs11249512	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11249513	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11249515	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1159714	0.90[EUR][1000 genomes]
rs1159715	0.90[EUR][1000 genomes]
rs11736796	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11936412	0.82[EUR][1000 genomes]
rs11940320	0.82[EUR][1000 genomes]
rs11946857	0.92[EUR][1000 genomes]
rs12499093	0.82[EUR][1000 genomes]
rs12508920	0.82[EUR][1000 genomes]
rs12509040	0.80[EUR][1000 genomes]
rs12509066	0.92[EUR][1000 genomes]
rs12510036	0.82[EUR][1000 genomes]
rs1303726	0.84[AFR][1000 genomes]
rs13104293	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13106664	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13113544	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13128286	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13128843	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13132528	0.89[EUR][1000 genomes]
rs13148179	0.90[EUR][1000 genomes]
rs13148603	0.89[EUR][1000 genomes]
rs1379813	0.89[EUR][1000 genomes]
rs1379816	0.89[EUR][1000 genomes]
rs1458236	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1458237	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1458242	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1458243	0.88[EUR][1000 genomes]
rs1458245	0.89[EUR][1000 genomes]
rs1458246	0.89[EUR][1000 genomes]
rs1598904	0.89[EUR][1000 genomes]
rs17605102	0.81[EUR][1000 genomes]
rs1902925	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1902926	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1902927	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1902928	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1962953	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1989329	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1993546	0.82[EUR][1000 genomes]
rs1993547	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2009312	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2017125	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2018150	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2125305	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2168840	0.92[EUR][1000 genomes]
rs2168841	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2331561	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2331562	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2331577	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs3088249	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3749511	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs3749513	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3828504	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs3966087	0.82[AFR][1000 genomes]
rs4412056	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4518317	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4694358	0.83[EUR][1000 genomes]
rs4694448	0.90[EUR][1000 genomes]
rs4694449	0.90[EUR][1000 genomes]
rs55647928	0.92[EUR][1000 genomes]
rs55795005	0.92[EUR][1000 genomes]
rs6600857	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6843537	0.90[EUR][1000 genomes]
rs6843550	0.92[EUR][1000 genomes]
rs6847539	0.86[EUR][1000 genomes]
rs6849125	0.82[EUR][1000 genomes]
rs6858791	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7441753	0.89[EUR][1000 genomes]
rs7666446	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7674475	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7688541	0.83[AFR][1000 genomes]
rs7692753	0.88[EUR][1000 genomes]
rs9329037	0.88[EUR][1000 genomes]
rs969338	0.90[EUR][1000 genomes]
rs994229	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9996467	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9999996	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005513	chr4:69446718-69890307	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv999654	chr4:69661415-70132110	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
3	esv3420586	chr4:69680878-70322918	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
4	esv3398036	chr4:69700493-69841391	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv1067773	chr4:69718248-70715727	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	esv3468151	chr4:69718675-70322776	Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
7	esv3468153	chr4:69718675-70322776	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
8	nsv436447	chr4:69743339-69851390	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv4372	chr4:69764499-69810115	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv967757	chr4:69780530-69790564	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv967758	chr4:69780530-69870183	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr4:69781200-69786400	Weak transcription	Fetal Intestine Small	intestine

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