Variant report

Variant	rs1933764
Chromosome Location	chr6:130855495-130855496
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1203340	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1203341	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1203342	0.96[ASN][1000 genomes]
rs1203343	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1203344	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1203345	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1203346	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1203347	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1203348	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs12526873	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1933759	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1933765	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1933766	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1933767	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1933768	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2326916	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2876084	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4897429	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6569688	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6940599	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs766966	0.80[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs766967	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9321230	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9375731	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9388802	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][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	nsv533971	chr6:130490694-131172051	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:130848800-130856200	Weak transcription	NHEK	skin
2	chr6:130851400-130856000	Weak transcription	HMEC	breast
3	chr6:130854600-130855600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr6:130855000-130857600	Weak transcription	Primary T cells from cord blood	blood
5	chr6:130855200-130858200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr6:130855400-130857000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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