Variant report

Variant	rs6904687
Chromosome Location	chr6:102121981-102121982
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10485273	0.94[CHB][hapmap];0.81[JPT][hapmap];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10872738	1.00[CHB][hapmap];0.85[JPT][hapmap];0.87[YRI][hapmap]
rs10872739	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1222958	0.87[CHB][hapmap];0.86[ASN][1000 genomes]
rs1222960	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1337412	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1337415	0.93[CEU][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1337424	0.88[CEU][hapmap];0.94[CHB][hapmap]
rs1415485	0.89[CHB][hapmap]
rs1415489	0.93[CEU][hapmap];0.94[CHB][hapmap];0.81[JPT][hapmap];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1832293	0.94[CHB][hapmap];0.91[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2065938	0.93[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap]
rs2105118	0.94[CEU][hapmap];0.88[CHB][hapmap];0.88[YRI][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2225865	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2248660	0.86[YRI][hapmap]
rs2518294	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2518295	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2518303	0.93[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2786251	0.93[CEU][hapmap];0.94[CHB][hapmap]
rs2786254	0.94[CHB][hapmap];0.91[JPT][hapmap]
rs2852560	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2852565	0.88[CEU][hapmap];0.87[CHB][hapmap]
rs2852566	0.82[YRI][hapmap]
rs4839800	0.93[CEU][hapmap];0.94[CHB][hapmap];0.81[JPT][hapmap]
rs6923409	0.94[CHB][hapmap];0.90[JPT][hapmap]
rs9322602	1.00[CHB][hapmap];0.90[JPT][hapmap];0.88[YRI][hapmap];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9322603	0.88[CEU][hapmap];1.00[CHB][hapmap]
rs9390768	0.89[CHB][hapmap]
rs9399725	0.83[YRI][hapmap]
rs9485526	0.83[CHB][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9485528	0.80[CEU][hapmap];0.93[YRI][hapmap]
rs9485530	1.00[CHB][hapmap];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9485532	0.94[ASN][1000 genomes]
rs9498658	0.84[CHB][hapmap];0.82[YRI][hapmap];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9498659	0.83[CHB][hapmap];0.81[ASN][1000 genomes]
rs9498662	0.84[CHB][hapmap];0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9498663	0.89[CHB][hapmap];0.91[JPT][hapmap];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9498664	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9498667	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv538392	chr6:101938381-102148360	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv3384771	chr6:101996253-102283808	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1032499	chr6:102069885-102720998	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv463993	chr6:102084491-102165329	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv604317	chr6:102084491-102165329	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	1 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