Variant report

Variant	rs17429055
Chromosome Location	chr5:113522851-113522852
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10045738	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10066191	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10078772	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11747036	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17350454	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2974468	0.93[ASN][1000 genomes]
rs4260657	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4272124	0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4365834	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4368718	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4416597	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4519916	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4537051	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4583880	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4612056	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4705487	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4705488	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4705625	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4705626	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4705628	0.89[EUR][1000 genomes]
rs62382864	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62382892	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6594791	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6594793	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6871846	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6873105	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6873190	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6875528	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6879669	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7720919	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7721332	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7721339	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9326911	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882726	chr5:113404933-113555626	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv2763899	chr5:113474771-113533857	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv599432	chr5:113486177-113561766	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv965569	chr5:113515560-113527423	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113521200-113526600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr5:113521600-113526400	Weak transcription	Fetal Heart	heart
3	chr5:113522000-113527200	Weak transcription	NHEK	skin

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