Variant report

Variant	rs10062331
Chromosome Location	chr5:15152798-15152799
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs10042846	0.84[ASN][1000 genomes]
rs10059252	0.84[ASN][1000 genomes]
rs10059362	0.84[ASN][1000 genomes]
rs10059428	0.83[ASN][1000 genomes]
rs10061831	0.84[ASN][1000 genomes]
rs10070527	0.86[ASN][1000 genomes]
rs10073782	0.84[ASN][1000 genomes]
rs10075680	0.84[ASN][1000 genomes]
rs10078235	0.86[ASN][1000 genomes]
rs1027577	0.85[ASN][1000 genomes]
rs10475039	0.86[ASN][1000 genomes]
rs10475040	0.86[ASN][1000 genomes]
rs10475044	0.84[ASN][1000 genomes]
rs10513204	0.84[ASN][1000 genomes]
rs11133805	0.84[ASN][1000 genomes]
rs1122149	0.84[ASN][1000 genomes]
rs1122150	0.84[ASN][1000 genomes]
rs1160025	0.93[ASN][1000 genomes]
rs12716107	0.86[ASN][1000 genomes]
rs13167378	0.84[ASN][1000 genomes]
rs13182271	0.91[ASN][1000 genomes]
rs1466014	0.84[ASN][1000 genomes]
rs1500229	0.84[ASN][1000 genomes]
rs1500230	0.84[ASN][1000 genomes]
rs1500231	0.84[ASN][1000 genomes]
rs167292	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs168694	0.84[ASN][1000 genomes]
rs173556	0.84[ASN][1000 genomes]
rs173557	0.84[ASN][1000 genomes]
rs2044421	0.84[ASN][1000 genomes]
rs2044422	0.84[ASN][1000 genomes]
rs2121181	0.86[ASN][1000 genomes]
rs2166391	0.86[ASN][1000 genomes]
rs2197527	0.84[ASN][1000 genomes]
rs2197529	0.84[ASN][1000 genomes]
rs2218529	0.84[ASN][1000 genomes]
rs2218532	0.84[ASN][1000 genomes]
rs2402051	0.86[ASN][1000 genomes]
rs2402052	0.84[ASN][1000 genomes]
rs2438384	0.81[ASN][1000 genomes]
rs2445896	0.84[ASN][1000 genomes]
rs2454881	0.84[ASN][1000 genomes]
rs2454882	0.84[ASN][1000 genomes]
rs2454883	0.84[ASN][1000 genomes]
rs2454885	0.84[ASN][1000 genomes]
rs248144	0.84[ASN][1000 genomes]
rs248146	0.84[ASN][1000 genomes]
rs248148	0.84[ASN][1000 genomes]
rs248149	0.84[ASN][1000 genomes]
rs248151	0.84[ASN][1000 genomes]
rs248152	0.84[ASN][1000 genomes]
rs248153	0.84[ASN][1000 genomes]
rs248154	0.82[ASN][1000 genomes]
rs2577991	0.83[ASN][1000 genomes]
rs2577993	0.83[ASN][1000 genomes]
rs2607527	0.83[ASN][1000 genomes]
rs2607528	0.94[CHB][hapmap];0.86[JPT][hapmap]
rs2937082	0.84[ASN][1000 genomes]
rs35730620	0.83[ASN][1000 genomes]
rs41013	0.84[ASN][1000 genomes]
rs412659	0.84[ASN][1000 genomes]
rs4282310	0.86[ASN][1000 genomes]
rs434412	0.84[ASN][1000 genomes]
rs4554219	0.98[ASN][1000 genomes]
rs4563625	0.84[ASN][1000 genomes]
rs509268	0.94[CHB][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs6554873	0.84[ASN][1000 genomes]
rs6554874	0.84[ASN][1000 genomes]
rs6554875	0.84[ASN][1000 genomes]
rs6865990	0.84[ASN][1000 genomes]
rs6872754	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6873820	0.84[ASN][1000 genomes]
rs692944	0.83[ASN][1000 genomes]
rs7713564	0.86[ASN][1000 genomes]
rs7716298	0.84[ASN][1000 genomes]
rs7721868	0.98[ASN][1000 genomes]
rs7727276	0.83[ASN][1000 genomes]
rs9284959	0.86[ASN][1000 genomes]
rs9312880	0.84[ASN][1000 genomes]
rs9654448	0.84[ASN][1000 genomes]
rs9654449	0.84[ASN][1000 genomes]
rs9654450	0.84[ASN][1000 genomes]
rs977760	0.98[ASN][1000 genomes]
rs977762	0.95[ASN][1000 genomes]
rs977763	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530221	chr5:14859687-15364470	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
2	nsv1017579	chr5:14888997-15194335	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv516929	chr5:15087791-15870300	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv1023068	chr5:15095221-15863583	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats 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	13 gene(s)	inside rSNPs	diseases
5	nsv869040	chr5:15097602-15866117	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv881665	chr5:15149009-15317509	Enhancers Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv530222	chr5:15151662-15851485	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr5:15152600-15155200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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