Variant report

Variant	rs9692914
Chromosome Location	chr8:42545296-42545297
allele	C/T
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:40)

rs_ID	r²[population]
rs10958725	0.86[AFR][1000 genomes]
rs10958727	0.82[EUR][1000 genomes]
rs13254578	0.82[EUR][1000 genomes]
rs13273442	0.84[EUR][1000 genomes]
rs13277254	0.81[EUR][1000 genomes]
rs13277524	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13280604	0.82[EUR][1000 genomes]
rs1451239	0.82[EUR][1000 genomes]
rs1451240	0.82[EUR][1000 genomes]
rs16891561	0.81[EUR][1000 genomes]
rs1901281	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1955185	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1955186	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1979140	0.88[AFR][1000 genomes]
rs34456987	0.86[AFR][1000 genomes]
rs35599391	0.89[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs4236926	0.81[EUR][1000 genomes]
rs4295650	0.82[EUR][1000 genomes]
rs4736835	0.82[EUR][1000 genomes]
rs4736836	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4736838	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4950	0.82[EUR][1000 genomes]
rs4951	0.81[EUR][1000 genomes]
rs57645595	0.80[EUR][1000 genomes]
rs59519538	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6474411	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6474412	0.82[EUR][1000 genomes]
rs6474413	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6474414	0.82[EUR][1000 genomes]
rs6474415	0.81[EUR][1000 genomes]
rs6985052	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6997909	0.82[EUR][1000 genomes]
rs7004381	0.81[EUR][1000 genomes]
rs7842601	0.82[EUR][1000 genomes]
rs9643853	0.82[EUR][1000 genomes]
rs9643891	0.82[EUR][1000 genomes]
rs9693825	0.90[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs9693858	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9792257	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9792277	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530880	chr8:41895241-42755506	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv1034724	chr8:42386707-42772203	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
3	nsv1030451	chr8:42543326-42618390	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr8:42539200-42545400	Weak transcription	HepG2	liver
2	chr8:42544000-42561200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:42545200-42547800	Weak transcription	HSMM	muscle

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