Variant report

Variant	rs9342008
Chromosome Location	chr6:85861223-85861224
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs12213780	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12664883	0.82[ASN][1000 genomes]
rs1321723	0.80[ASN][1000 genomes]
rs1321734	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1321735	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1321736	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1321737	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1407159	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1407160	0.81[ASN][1000 genomes]
rs1407161	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1407162	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1885017	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1926019	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2146272	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4141965	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs486470	0.80[ASN][1000 genomes]
rs504392	0.80[ASN][1000 genomes]
rs505007	0.80[ASN][1000 genomes]
rs510422	0.80[ASN][1000 genomes]
rs536094	0.80[ASN][1000 genomes]
rs541665	0.82[ASN][1000 genomes]
rs562034	0.80[ASN][1000 genomes]
rs563365	0.82[ASN][1000 genomes]
rs563639	0.80[ASN][1000 genomes]
rs572893	0.82[ASN][1000 genomes]
rs575779	0.82[ASN][1000 genomes]
rs618586	0.95[CHB][hapmap]
rs633322	0.81[CHB][hapmap]
rs6454422	0.84[ASN][1000 genomes]
rs6454423	0.87[ASN][1000 genomes]
rs662760	0.83[CHB][hapmap]
rs6911391	0.96[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap]
rs6925525	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72624531	0.89[ASN][1000 genomes]
rs7745528	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7748912	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7768040	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9362128	0.87[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:0 , 50 per page) page:

No data

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links