Variant report

Variant	rs6769910
Chromosome Location	chr3:143737830-143737831
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:143735422..143737968-chr3:143770929..143772909,2	K562	blood:

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs1025984	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10513235	0.94[EUR][1000 genomes]
rs11914731	0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13067695	0.90[ASN][1000 genomes]
rs13068298	0.90[ASN][1000 genomes]
rs13078840	0.94[EUR][1000 genomes]
rs13081286	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13086088	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16854772	0.95[EUR][1000 genomes]
rs16854816	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16854819	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16854884	0.90[ASN][1000 genomes]
rs16854886	0.90[ASN][1000 genomes]
rs17667256	0.80[EUR][1000 genomes]
rs1867608	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1867609	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1898265	0.97[ASN][1000 genomes]
rs1961542	0.90[ASN][1000 genomes]
rs1979910	0.99[EUR][1000 genomes]
rs2011080	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2164554	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2370171	0.90[ASN][1000 genomes]
rs34372603	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34683397	0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35067746	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35085196	0.99[EUR][1000 genomes]
rs35193361	0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35309714	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35629416	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35649888	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35788195	0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35796781	0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35877644	0.95[EUR][1000 genomes]
rs35885310	0.97[ASN][1000 genomes]
rs35887108	0.90[ASN][1000 genomes]
rs35959290	0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4527375	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4561830	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4611822	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4613453	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4616638	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56196484	0.80[ASN][1000 genomes]
rs59768870	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs60367530	0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs60676654	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62268458	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62269895	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6440210	0.98[EUR][1000 genomes]
rs6440212	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6766544	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6766685	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6767236	0.90[ASN][1000 genomes]
rs6778627	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6779321	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6783089	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6791078	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6795008	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6796460	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7611326	0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7634145	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7637912	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7639366	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7642551	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7642774	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7646187	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7650145	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7650172	0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs920159	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9755502	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9755515	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877568	chr3:143621140-143992630	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	esv3365190	chr3:143642195-143925886	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv591922	chr3:143645242-143825439	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143736800-143738400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr3:143736800-143738400	Enhancers	HSMM	muscle
3	chr3:143737400-143738000	Enhancers	HMEC	breast
4	chr3:143737400-143738200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr3:143737400-143738400	Enhancers	Muscle Satellite Cultured Cells	--
6	chr3:143737600-143738000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr3:143737600-143738200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr3:143737600-143738200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr3:143737600-143738200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr3:143737600-143738200	Enhancers	Placenta Amnion	Placenta Amnion
11	chr3:143737600-143738200	Enhancers	HSMMtube	muscle
12	chr3:143737600-143738200	Enhancers	NH-A	brain
13	chr3:143737600-143738400	Enhancers	Osteobl	bone
14	chr3:143737600-143739200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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