Variant report

Variant	rs10009372
Chromosome Location	chr4:62996166-62996167
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10008066	0.90[EUR][1000 genomes]
rs10027730	0.95[ASN][1000 genomes]
rs10033607	0.91[EUR][1000 genomes]
rs11131356	0.81[ASN][1000 genomes]
rs11930426	0.91[EUR][1000 genomes]
rs11944228	0.91[EUR][1000 genomes]
rs12500654	0.91[EUR][1000 genomes]
rs12507188	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12511066	0.85[EUR][1000 genomes]
rs13121574	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17226468	0.80[ASN][1000 genomes]
rs1990690	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap]
rs1990691	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2216195	0.90[EUR][1000 genomes]
rs2216197	1.00[CEU][hapmap];0.95[CHB][hapmap];0.85[JPT][hapmap]
rs2287146	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs28615650	0.86[EUR][1000 genomes]
rs28661220	0.85[EUR][1000 genomes]
rs28819240	0.91[EUR][1000 genomes]
rs4277807	0.86[EUR][1000 genomes]
rs4282218	0.86[EUR][1000 genomes]
rs4860451	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6551676	0.91[EUR][1000 genomes]
rs6551680	0.90[EUR][1000 genomes]
rs6551681	0.90[EUR][1000 genomes]
rs6551683	0.94[CEU][hapmap]
rs6810664	0.90[EUR][1000 genomes]
rs6827497	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6833025	0.91[EUR][1000 genomes]
rs6836463	0.86[EUR][1000 genomes]
rs6848354	0.91[EUR][1000 genomes]
rs6857895	0.91[EUR][1000 genomes]
rs7657624	0.82[EUR][1000 genomes]
rs7662331	0.88[EUR][1000 genomes]
rs7664142	0.86[EUR][1000 genomes]
rs7671439	0.86[EUR][1000 genomes]
rs7677634	0.90[EUR][1000 genomes]
rs7682584	0.90[EUR][1000 genomes]
rs7692875	0.86[EUR][1000 genomes]
rs7695511	0.86[EUR][1000 genomes]
rs7697748	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs950313	0.90[EUR][1000 genomes]
rs9995712	0.86[EUR][1000 genomes]
rs9999509	0.91[EUR][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	nsv879078	chr4:62923797-63054757	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv594332	chr4:62976756-63034074	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1005620	chr4:62978115-63035387	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription	TF binding region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1013327	chr4:62989426-63149048	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr4:62995800-62996200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:62995800-62996800	Enhancers	Fetal Heart	heart
3	chr4:62996000-62996800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links