Variant report

Variant	rs443272
Chromosome Location	chr5:94610761-94610762
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10050382	0.80[EUR][1000 genomes]
rs10057040	0.82[EUR][1000 genomes]
rs10058623	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10060946	0.81[EUR][1000 genomes]
rs10066492	0.82[EUR][1000 genomes]
rs10068165	0.81[EUR][1000 genomes]
rs10068954	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10515223	0.82[EUR][1000 genomes]
rs154056	0.84[ASN][1000 genomes]
rs154057	0.84[ASN][1000 genomes]
rs154062	0.82[CEU][hapmap]
rs154063	0.88[CEU][hapmap];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs154064	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs154066	0.81[AMR][1000 genomes]
rs255979	0.84[ASN][1000 genomes]
rs255980	0.81[ASN][1000 genomes]
rs255981	0.84[ASN][1000 genomes]
rs255983	0.84[ASN][1000 genomes]
rs255984	0.84[ASN][1000 genomes]
rs255985	0.84[ASN][1000 genomes]
rs255986	0.84[ASN][1000 genomes]
rs255987	0.83[ASN][1000 genomes]
rs26393	0.80[CHB][hapmap];0.88[ASN][1000 genomes]
rs26394	0.88[ASN][1000 genomes]
rs26395	0.80[CHB][hapmap];0.91[CHD][hapmap];0.81[GIH][hapmap];0.88[ASN][1000 genomes]
rs27688	0.81[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs27767	0.80[CEU][hapmap];0.80[CHB][hapmap];0.88[ASN][1000 genomes]
rs27768	0.81[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap]
rs3104738	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs33810	0.89[ASN][1000 genomes]
rs33811	0.80[CHB][hapmap];0.86[CHD][hapmap];1.00[MEX][hapmap];0.88[ASN][1000 genomes]
rs33813	0.88[ASN][1000 genomes]
rs395031	0.84[ASN][1000 genomes]
rs397826	0.82[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs421754	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs448433	0.80[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs455516	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs457568	0.84[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs457819	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs458134	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs458663	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs458978	0.88[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs459730	0.88[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs460102	0.82[CEU][hapmap];0.90[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs460363	0.82[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs460924	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs461018	0.89[ASN][1000 genomes]
rs461059	0.88[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs462526	0.80[CEU][hapmap];0.89[JPT][hapmap];0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs462828	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs462862	0.81[CEU][hapmap];0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs463261	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs463587	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs463961	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs464001	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs464008	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs464084	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs464158	0.81[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs464242	0.87[CEU][hapmap]
rs464906	1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[JPT][hapmap];0.97[ASN][1000 genomes]
rs464971	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs465847	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs466024	0.82[CEU][hapmap]
rs467144	0.82[CEU][hapmap];0.90[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.90[ASN][1000 genomes]
rs669335	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs686420	0.88[CEU][hapmap]
rs73776337	0.82[EUR][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	nsv432752	chr5:94524244-94691044	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94602400-94616200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr5:94609600-94611200	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr5:94609800-94610800	Enhancers	Monocytes-CD14+_RO01746	blood

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