Variant report

Variant	rs612117
Chromosome Location	chr6:101344511-101344512
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11155726	1.00[ASN][1000 genomes]
rs12189857	1.00[ASN][1000 genomes]
rs17061209	1.00[CHB][hapmap];0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17061230	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17673031	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2749130	1.00[ASN][1000 genomes]
rs2756040	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4615398	1.00[ASN][1000 genomes]
rs4839795	1.00[ASN][1000 genomes]
rs592463	1.00[ASN][1000 genomes]
rs596601	1.00[CHB][hapmap]
rs600653	1.00[ASN][1000 genomes]
rs601360	1.00[ASN][1000 genomes]
rs606032	1.00[ASN][1000 genomes]
rs609522	0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs612459	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs613338	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs614094	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs614097	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs617365	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs625745	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs626120	0.87[YRI][hapmap]
rs626411	1.00[ASN][1000 genomes]
rs635258	1.00[ASN][1000 genomes]
rs640315	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs668932	0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs673138	1.00[ASN][1000 genomes]
rs674589	1.00[ASN][1000 genomes]
rs705594	1.00[ASN][1000 genomes]
rs705595	1.00[ASN][1000 genomes]
rs705598	0.85[ASW][hapmap];1.00[CHB][hapmap];0.92[LWK][hapmap];1.00[ASN][1000 genomes]
rs705601	1.00[ASN][1000 genomes]
rs705602	1.00[ASN][1000 genomes]
rs705609	1.00[CHB][hapmap];0.88[LWK][hapmap];1.00[ASN][1000 genomes]
rs705612	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs705618	1.00[ASN][1000 genomes]
rs72944877	1.00[ASN][1000 genomes]
rs72946427	1.00[ASN][1000 genomes]
rs72947091	1.00[ASN][1000 genomes]
rs72951137	1.00[ASN][1000 genomes]
rs72951161	1.00[ASN][1000 genomes]
rs7755696	1.00[ASN][1000 genomes]
rs817226	1.00[ASN][1000 genomes]
rs817227	1.00[ASN][1000 genomes]
rs817234	1.00[ASN][1000 genomes]
rs846784	1.00[ASN][1000 genomes]
rs846790	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs861752	1.00[ASN][1000 genomes]
rs9390724	1.00[ASN][1000 genomes]
rs9498487	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 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	nsv1020692	chr6:101136992-101426071	ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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
6	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
7	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
8	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:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:101340800-101345400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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