Variant report

Variant	rs4589964
Chromosome Location	chr3:105067443-105067444
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs13065937	0.87[CHB][hapmap]
rs13070790	0.91[CHB][hapmap]
rs13075944	0.83[CHB][hapmap]
rs13079517	0.86[CHB][hapmap]
rs13085657	0.86[CHB][hapmap]
rs13092913	0.86[CHB][hapmap]
rs13095216	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs13095274	0.83[ASN][1000 genomes]
rs1438544	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1438546	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1438549	0.91[CHB][hapmap]
rs1438551	0.87[CHB][hapmap]
rs1438553	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1438554	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16851175	0.86[CHB][hapmap]
rs2399046	0.91[CHB][hapmap]
rs4894926	0.87[CHB][hapmap]
rs55934921	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62262153	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6437579	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6437582	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6437583	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6437584	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6773531	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6793758	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6797065	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6797259	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6804633	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7611398	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7620029	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7620713	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7626665	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7634168	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7635959	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9288801	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs976530	0.87[CHB][hapmap]
rs9852729	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9869867	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9880342	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9883403	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525071	chr3:105004853-105409321	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:105066800-105067600	Enhancers	Monocytes-CD14+_RO01746	blood
2	chr3:105067400-105067600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr3:105067400-105068000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr3:105067400-105068000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr3:105067400-105069800	Weak transcription	Primary monocytes fromperipheralblood	blood

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