Variant report

Variant	rs17254611
Chromosome Location	chr4:173898334-173898335
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10003998	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10014915	0.84[EUR][1000 genomes]
rs10520249	0.88[CEU][hapmap]
rs10520251	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap]
rs12641678	0.82[CEU][hapmap];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12644630	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17254079	0.88[CEU][hapmap];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17254681	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17319595	0.82[CEU][hapmap]
rs2610188	0.88[CEU][hapmap];0.83[ASN][1000 genomes]
rs2610191	0.83[ASN][1000 genomes]
rs2653844	0.88[CEU][hapmap];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28380538	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28483480	0.88[EUR][1000 genomes]
rs28485277	0.85[EUR][1000 genomes]
rs28524136	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28582871	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28671519	0.87[EUR][1000 genomes]
rs28705797	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28800549	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28890012	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4547777	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55936404	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56110146	0.83[ASN][1000 genomes]
rs62341884	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62341886	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62341887	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62341919	0.82[EUR][1000 genomes]
rs62341920	0.80[EUR][1000 genomes]
rs6553660	0.85[CEU][hapmap]
rs6852770	0.82[CEU][hapmap];0.83[ASN][1000 genomes]
rs7663630	0.88[EUR][1000 genomes]
rs7678191	0.84[CEU][hapmap]
rs7682619	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7693329	0.94[CEU][hapmap];0.88[EUR][1000 genomes]
rs9997573	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv948856	chr4:173388217-173967546	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv949126	chr4:173466221-174051451	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:173896200-173899600	Weak transcription	Gastric	stomach
2	chr4:173897200-173901800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr4:173897800-173899400	Enhancers	A549	lung
4	chr4:173898000-173898800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr4:173898000-173904200	Enhancers	Hela-S3	cervix
6	chr4:173898200-173898800	Enhancers	HMEC	breast

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