Variant report

Variant	rs73182758
Chromosome Location	chr3:19398241-19398242
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11128915	0.87[ASN][1000 genomes]
rs12107127	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12108118	0.91[AFR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12632920	0.92[ASN][1000 genomes]
rs12633153	0.90[ASN][1000 genomes]
rs12635216	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1442195	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17005851	0.85[AFR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17005867	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28456201	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28488710	0.86[ASN][1000 genomes]
rs4425284	0.82[AFR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56256260	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58411951	0.91[AFR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6768477	0.88[AFR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73182727	0.87[ASN][1000 genomes]
rs73182734	0.90[ASN][1000 genomes]
rs73182739	0.91[ASN][1000 genomes]
rs73182741	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73182745	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73182749	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73182755	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73818294	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73819514	0.87[ASN][1000 genomes]
rs7431348	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs956380	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9812170	0.91[ASN][1000 genomes]
rs9827197	0.91[ASN][1000 genomes]
rs9827599	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9831335	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9834735	0.87[ASN][1000 genomes]
rs9843179	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9843569	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9859268	0.90[ASN][1000 genomes]
rs9865301	0.82[AFR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9865551	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9865785	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9875776	0.81[EUR][1000 genomes];0.94[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	nsv517847	chr3:18845347-19483695	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1010123	chr3:18990307-19989504	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv1004602	chr3:19031671-19930052	Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv536511	chr3:19031671-19930052	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv948636	chr3:19335802-19856585	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:19391200-19402800	Weak transcription	Primary B cells from cord blood	blood
2	chr3:19395200-19423800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links