Variant report

Variant	rs1885017
Chromosome Location	chr6:85845426-85845427
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs12213780	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1321734	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1321735	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1321736	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1321737	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1407159	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1407161	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1407162	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1926019	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2146272	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4141965	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs618586	1.00[CHB][hapmap]
rs633322	0.85[CHB][hapmap]
rs6454422	0.86[ASN][1000 genomes]
rs6454423	0.86[ASN][1000 genomes]
rs662760	0.86[CHB][hapmap]
rs6911391	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap]
rs6925525	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72624531	0.84[ASN][1000 genomes]
rs7745528	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7748912	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7768040	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9342008	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9362128	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017418	chr6:85344786-86259540	Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv538347	chr6:85344786-86259540	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:85837600-85845600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr6:85843000-85846800	Enhancers	Osteobl	bone
3	chr6:85843600-85846000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr6:85844400-85849800	Enhancers	NHDF-Ad	bronchial
5	chr6:85844600-85848200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr6:85844800-85845600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr6:85844800-85846400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr6:85845000-85846200	Enhancers	HSMMtube	muscle
9	chr6:85845200-85846800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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