Variant report

Variant	rs667338
Chromosome Location	chr3:109658843-109658844
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1164227	0.88[ASN][1000 genomes]
rs2682531	0.95[ASN][1000 genomes]
rs2693620	0.96[ASN][1000 genomes]
rs2693635	0.96[ASN][1000 genomes]
rs2700255	0.96[ASN][1000 genomes]
rs2700258	1.00[ASN][1000 genomes]
rs3915171	0.88[ASN][1000 genomes]
rs594096	0.82[ASN][1000 genomes]
rs597310	0.88[ASN][1000 genomes]
rs600054	0.91[ASN][1000 genomes]
rs603148	0.96[ASN][1000 genomes]
rs604438	0.94[ASN][1000 genomes]
rs604985	0.92[ASN][1000 genomes]
rs605347	0.85[ASN][1000 genomes]
rs605413	0.83[ASN][1000 genomes]
rs605451	0.85[ASN][1000 genomes]
rs605810	0.82[ASN][1000 genomes]
rs606216	1.00[ASN][1000 genomes]
rs612254	1.00[ASN][1000 genomes]
rs614450	1.00[ASN][1000 genomes]
rs614804	0.99[ASN][1000 genomes]
rs617517	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs618829	0.96[ASN][1000 genomes]
rs623226	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs626977	1.00[ASN][1000 genomes]
rs627434	1.00[ASN][1000 genomes]
rs632144	0.95[ASN][1000 genomes]
rs642983	1.00[ASN][1000 genomes]
rs654027	0.96[ASN][1000 genomes]
rs654076	0.96[ASN][1000 genomes]
rs654095	0.96[ASN][1000 genomes]
rs656177	0.85[ASN][1000 genomes]
rs657025	1.00[ASN][1000 genomes]
rs657834	1.00[ASN][1000 genomes]
rs664861	1.00[ASN][1000 genomes]
rs666129	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs666533	0.96[ASN][1000 genomes]
rs666674	1.00[ASN][1000 genomes]
rs671574	1.00[ASN][1000 genomes]
rs672489	1.00[ASN][1000 genomes]
rs673959	1.00[ASN][1000 genomes]
rs678058	0.88[ASN][1000 genomes]
rs680451	0.88[ASN][1000 genomes]
rs684185	0.82[ASN][1000 genomes]
rs686071	0.90[ASN][1000 genomes]
rs686207	0.96[ASN][1000 genomes]
rs687955	1.00[ASN][1000 genomes]
rs688616	0.82[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	nsv1009075	chr3:109462019-109800029	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv591270	chr3:109462400-109793785	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv877332	chr3:109575764-110186611	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1009550	chr3:109577315-109795453	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv1839660	chr3:109591203-109678542	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv829666	chr3:109593745-109768652	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	esv2754434	chr3:109604310-109777310	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr3:109658600-109659200	Enhancers	Muscle Satellite Cultured Cells	--

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