Variant report

Variant	rs2044654
Chromosome Location	chr3:85783923-85783924
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10084716	0.84[JPT][hapmap]
rs10511074	0.83[CEU][hapmap];1.00[CHB][hapmap]
rs11127905	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11711972	1.00[JPT][hapmap]
rs12494196	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1375218	0.87[JPT][hapmap]
rs1375219	0.86[JPT][hapmap]
rs1448607	0.84[JPT][hapmap]
rs1448616	0.86[JPT][hapmap]
rs17334733	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1947180	1.00[CEU][hapmap];0.84[CHB][hapmap];0.86[JPT][hapmap];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2017676	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2029051	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2029052	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2029053	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2325036	1.00[JPT][hapmap]
rs2325037	1.00[JPT][hapmap]
rs3901898	0.86[JPT][hapmap]
rs3930071	0.86[JPT][hapmap]
rs4129298	0.89[EUR][1000 genomes]
rs4298053	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4302392	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4305433	0.94[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap]
rs4312666	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4320069	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4435654	0.94[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap]
rs4482674	0.82[EUR][1000 genomes]
rs4488844	0.86[JPT][hapmap]
rs4555536	1.00[JPT][hapmap]
rs4555539	0.86[JPT][hapmap]
rs4618235	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4856606	0.86[JPT][hapmap]
rs6549047	0.94[CEU][hapmap]
rs6549048	0.89[EUR][1000 genomes]
rs6549054	1.00[JPT][hapmap]
rs6549055	0.86[JPT][hapmap]
rs6781999	1.00[CEU][hapmap];0.83[CHB][hapmap];0.86[JPT][hapmap];0.89[EUR][1000 genomes]
rs6787901	0.86[JPT][hapmap]
rs6796380	0.86[JPT][hapmap]
rs6796402	0.87[JPT][hapmap]
rs6799453	1.00[JPT][hapmap]
rs73142855	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73147238	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73147239	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73147242	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7611409	1.00[JPT][hapmap]
rs7612371	1.00[JPT][hapmap]
rs7615964	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs7624423	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7637221	0.87[JPT][hapmap]
rs7638774	1.00[JPT][hapmap]
rs7642281	0.86[JPT][hapmap]
rs7653470	1.00[JPT][hapmap]
rs9309992	0.86[JPT][hapmap]
rs9681744	1.00[JPT][hapmap]
rs9820133	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9820262	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9836755	1.00[JPT][hapmap]
rs9843797	1.00[JPT][hapmap]
rs9844720	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9851502	0.86[JPT][hapmap]
rs9860249	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap]
rs9864042	1.00[JPT][hapmap]
rs9876664	1.00[JPT][hapmap]
rs9878917	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9881886	1.00[JPT][hapmap]

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	nsv590905	chr3:85438564-85797093	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv1010541	chr3:85505839-85870597	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv536625	chr3:85505839-85870597	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1005102	chr3:85729640-85829412	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
5	nsv532629	chr3:85763873-86608579	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 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