Variant report

Variant	rs34847081
Chromosome Location	chr6:145689602-145689603
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10223879	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11155417	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12661545	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1856266	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1970320	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1970321	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2039698	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35270275	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4142213	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4896795	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4896796	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4896799	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6922610	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9373455	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9376921	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9376922	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9376924	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9376933	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9390310	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9390311	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9390314	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9390315	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9399545	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9403692	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9403694	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9403696	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9484987	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9497280	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9497287	0.93[AMR][1000 genomes];0.97[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	nsv1017166	chr6:145677071-145808448	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145688400-145692800	Weak transcription	GM12878-XiMat	blood
2	chr6:145689400-145690000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:145689400-145690000	Enhancers	Fetal Heart	heart
4	chr6:145689600-145694200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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