Variant report

Variant	rs7572637
Chromosome Location	chr2:213508377-213508378
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10174150	0.88[ASN][1000 genomes]
rs10198723	0.86[EUR][1000 genomes]
rs10221625	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10221626	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11676391	0.88[ASN][1000 genomes]
rs11687307	0.86[EUR][1000 genomes]
rs11688976	0.80[ASN][1000 genomes]
rs11692809	0.88[ASN][1000 genomes]
rs11695521	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11896992	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1320116	0.81[EUR][1000 genomes]
rs13386921	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13394068	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13395632	0.85[ASN][1000 genomes]
rs13397735	0.86[EUR][1000 genomes]
rs13404902	0.83[EUR][1000 genomes]
rs13422625	0.84[EUR][1000 genomes]
rs13431135	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13431628	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1384297	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1600883	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1600884	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2054613	0.88[ASN][1000 genomes]
rs2054615	0.88[ASN][1000 genomes]
rs2068404	0.88[ASN][1000 genomes]
rs2128324	0.88[ASN][1000 genomes]
rs2220026	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2371710	0.92[ASN][1000 genomes]
rs2888128	0.89[ASN][1000 genomes]
rs4337429	0.92[ASN][1000 genomes]
rs4673669	0.85[ASN][1000 genomes]
rs4673673	0.92[ASN][1000 genomes]
rs4673674	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4673675	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4673676	0.86[EUR][1000 genomes]
rs5000270	0.86[EUR][1000 genomes]
rs58184703	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62187963	0.86[EUR][1000 genomes]
rs62187964	0.86[EUR][1000 genomes]
rs62187967	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62187968	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6435715	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6435716	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6435717	0.87[EUR][1000 genomes]
rs6706987	0.88[ASN][1000 genomes]
rs6708862	0.86[ASN][1000 genomes]
rs6711917	0.86[ASN][1000 genomes]
rs6712252	0.86[ASN][1000 genomes]
rs6731808	0.82[ASN][1000 genomes]
rs6742665	0.86[EUR][1000 genomes]
rs6743091	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6749009	0.88[ASN][1000 genomes]
rs6749157	0.88[ASN][1000 genomes]
rs6750857	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs67535717	0.88[ASN][1000 genomes]
rs6761880	0.88[ASN][1000 genomes]
rs72933003	0.92[ASN][1000 genomes]
rs72933004	0.92[ASN][1000 genomes]
rs72933008	0.92[ASN][1000 genomes]
rs72951177	0.89[ASN][1000 genomes]
rs72951178	0.89[ASN][1000 genomes]
rs7583787	0.82[ASN][1000 genomes]
rs7585465	0.88[ASN][1000 genomes]
rs7587236	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7590349	0.86[EUR][1000 genomes]
rs7590700	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7598633	0.82[ASN][1000 genomes]
rs7601545	0.88[ASN][1000 genomes]
rs7606156	0.88[ASN][1000 genomes]
rs9288455	0.85[ASN][1000 genomes]
rs9967727	0.85[EUR][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	nsv948878	chr2:213345197-213534298	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv875813	chr2:213480637-213509809	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213505800-213509200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:213505800-213509400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:213505800-213511200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:213505800-213511200	Weak transcription	HMEC	breast
5	chr2:213505800-213511200	Weak transcription	NHEK	skin

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