Variant report

Variant	rs10059738
Chromosome Location	chr5:111278176-111278177
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs10045865	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10063079	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10463623	0.94[ASN][1000 genomes]
rs10463624	0.94[ASN][1000 genomes]
rs11241145	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11241146	0.92[ASN][1000 genomes]
rs12187912	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12187919	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13169766	0.89[ASN][1000 genomes]
rs13188104	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1493453	0.94[ASN][1000 genomes]
rs1493457	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1494585	0.95[ASN][1000 genomes]
rs1507846	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1603081	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1994871	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2017552	0.81[EUR][1000 genomes]
rs2047070	0.92[ASN][1000 genomes]
rs2048155	0.93[ASN][1000 genomes]
rs255910	0.81[ASN][1000 genomes]
rs255928	0.85[ASN][1000 genomes]
rs255929	0.82[ASN][1000 genomes]
rs255930	0.80[ASN][1000 genomes]
rs25791	0.92[EUR][1000 genomes]
rs25795	0.87[EUR][1000 genomes]
rs26539	0.86[ASN][1000 genomes]
rs26540	0.85[ASN][1000 genomes]
rs26541	0.86[ASN][1000 genomes]
rs26542	0.86[ASN][1000 genomes]
rs26543	0.89[ASN][1000 genomes]
rs26545	0.93[ASN][1000 genomes]
rs26557	0.88[ASN][1000 genomes]
rs26558	0.88[ASN][1000 genomes]
rs26559	0.84[ASN][1000 genomes]
rs26560	0.84[ASN][1000 genomes]
rs26561	0.85[ASN][1000 genomes]
rs26562	0.85[ASN][1000 genomes]
rs26563	0.85[ASN][1000 genomes]
rs27535	0.86[ASN][1000 genomes]
rs34924	0.89[ASN][1000 genomes]
rs34928	0.93[ASN][1000 genomes]
rs34930	0.93[ASN][1000 genomes]
rs34931	0.93[ASN][1000 genomes]
rs34941	0.82[ASN][1000 genomes]
rs34942	0.85[ASN][1000 genomes]
rs34942854	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35303575	0.94[ASN][1000 genomes]
rs35658682	0.95[ASN][1000 genomes]
rs36061964	0.89[ASN][1000 genomes]
rs36069145	0.94[ASN][1000 genomes]
rs36133922	0.94[ASN][1000 genomes]
rs41142	0.85[ASN][1000 genomes]
rs42308	0.93[ASN][1000 genomes]
rs474807	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs490983	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs491101	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4957626	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4957992	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4957993	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4957996	0.93[EUR][1000 genomes]
rs504582	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs508089	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs586262	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs593236	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs624694	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6878696	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6881837	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6882073	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6882205	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6890246	0.82[EUR][1000 genomes]
rs6898198	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs712660	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7708619	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7709592	0.85[EUR][1000 genomes]
rs7710690	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7712177	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7712346	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7716521	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7730997	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7735316	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9326846	0.94[ASN][1000 genomes]
rs980888	0.94[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv599367	chr5:110924280-111602713	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:111267200-111278600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr5:111272800-111278400	Weak transcription	NHEK	skin
3	chr5:111273800-111281400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr5:111274000-111278200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr5:111277400-111278200	Enhancers	Muscle Satellite Cultured Cells	--
6	chr5:111277400-111279400	Enhancers	HSMMtube	muscle
7	chr5:111277400-111279400	Enhancers	NHDF-Ad	bronchial
8	chr5:111277400-111279400	Enhancers	NHLF	lung
9	chr5:111278000-111279200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr5:111278000-111279200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr5:111278000-111279200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr5:111278000-111279400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr5:111278000-111279400	Enhancers	HMEC	breast
14	chr5:111278000-111279400	Enhancers	Osteobl	bone

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