Variant report

Variant	rs817234
Chromosome Location	chr6:101457707-101457708
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs11155726	1.00[ASN][1000 genomes]
rs12189857	1.00[ASN][1000 genomes]
rs1222375	1.00[ASN][1000 genomes]
rs17061209	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17061230	0.87[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17673031	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2254178	1.00[ASN][1000 genomes]
rs2399557	1.00[ASN][1000 genomes]
rs2749130	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2756040	0.87[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2764271	1.00[ASN][1000 genomes]
rs4240592	1.00[ASN][1000 genomes]
rs4429955	1.00[ASN][1000 genomes]
rs4455678	1.00[ASN][1000 genomes]
rs4615398	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4839795	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs592463	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs596601	1.00[CHB][hapmap]
rs600653	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs601360	1.00[ASN][1000 genomes]
rs606032	1.00[ASN][1000 genomes]
rs609522	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs612117	1.00[ASN][1000 genomes]
rs612459	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs613338	1.00[ASN][1000 genomes]
rs614097	1.00[ASN][1000 genomes]
rs617365	0.86[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs625745	0.86[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs626411	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs635258	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs640315	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs668932	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs673138	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs674589	1.00[ASN][1000 genomes]
rs705594	1.00[ASN][1000 genomes]
rs705595	1.00[ASN][1000 genomes]
rs705598	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs705601	1.00[ASN][1000 genomes]
rs705602	1.00[ASN][1000 genomes]
rs705609	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs705612	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs705618	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72942892	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72944877	1.00[ASN][1000 genomes]
rs72946427	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72947091	1.00[ASN][1000 genomes]
rs72951137	1.00[ASN][1000 genomes]
rs72951161	1.00[ASN][1000 genomes]
rs7740295	1.00[ASN][1000 genomes]
rs7755696	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs817226	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs817227	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs817228	0.81[EUR][1000 genomes]
rs846784	1.00[ASN][1000 genomes]
rs846790	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs846796	0.81[AMR][1000 genomes]
rs861752	1.00[ASN][1000 genomes]
rs9377258	0.81[AMR][1000 genomes]
rs9390724	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9498487	1.00[ASN][1000 genomes]
rs9498519	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949535	chr6:100740293-101469052	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv886457	chr6:101158950-101487473	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1020400	chr6:101172705-101981665	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv538390	chr6:101172705-101981665	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv1019213	chr6:101225650-101623140	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
6	nsv538391	chr6:101225650-101623140	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	esv2763587	chr6:101277874-101510491	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:101457400-101458600	Enhancers	Dnd41	blood
2	chr6:101457600-101458400	Enhancers	Fetal Brain Male	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links