Variant report

Variant	rs7742978
Chromosome Location	chr6:145302412-145302413
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1011291	0.88[AMR][1000 genomes]
rs11752326	0.83[EUR][1000 genomes]
rs12175554	0.94[AMR][1000 genomes]
rs13194942	0.96[EUR][1000 genomes]
rs13200093	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13216473	1.00[CEU][hapmap]
rs13216871	0.83[CEU][hapmap]
rs1338704	0.91[CEU][hapmap]
rs1338705	0.91[CEU][hapmap]
rs1416297	0.96[EUR][1000 genomes]
rs1572675	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1832481	0.80[EUR][1000 genomes]
rs2185145	0.96[EUR][1000 genomes]
rs2211068	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2328623	0.88[AMR][1000 genomes]
rs6570663	0.96[EUR][1000 genomes]
rs6932709	0.83[EUR][1000 genomes]
rs7769009	1.00[CEU][hapmap]
rs7773947	0.96[EUR][1000 genomes]
rs9322009	0.80[EUR][1000 genomes]
rs9322016	0.84[AMR][1000 genomes]
rs9322017	0.84[AMR][1000 genomes]
rs9373436	0.80[EUR][1000 genomes]
rs9373439	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9373440	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9373441	0.81[AMR][1000 genomes]
rs9376878	0.96[EUR][1000 genomes]
rs9376883	0.88[AMR][1000 genomes]
rs9376884	0.94[AMR][1000 genomes]
rs9376885	0.84[AMR][1000 genomes]
rs9376886	0.84[AMR][1000 genomes]
rs9376887	0.84[AMR][1000 genomes]
rs9386096	0.84[AMR][1000 genomes]
rs9386097	0.94[AMR][1000 genomes]
rs9390264	0.80[EUR][1000 genomes]
rs9390268	0.84[AMR][1000 genomes]
rs9390269	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9390270	0.82[AMR][1000 genomes]
rs9390271	0.88[AMR][1000 genomes]
rs9399523	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9399524	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9399525	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9399526	0.88[AMR][1000 genomes]
rs9403640	0.80[EUR][1000 genomes]
rs9403649	0.94[AMR][1000 genomes]
rs9403650	0.88[AMR][1000 genomes]
rs9403651	0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9403652	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9403653	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9403655	0.84[AMR][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	nsv1016747	chr6:144917411-145599874	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	esv1850377	chr6:145199259-145319640	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv886742	chr6:145269757-145376903	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145299000-145307400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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