Variant report

Variant	rs6545966
Chromosome Location	chr2:62861353-62861354
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10172216	0.90[ASN][1000 genomes]
rs10174703	0.91[ASN][1000 genomes]
rs10177638	0.82[ASN][1000 genomes]
rs10179232	0.89[ASN][1000 genomes]
rs11125941	0.84[ASN][1000 genomes]
rs11893614	0.90[ASN][1000 genomes]
rs13397831	0.80[ASN][1000 genomes]
rs13423306	0.88[ASN][1000 genomes]
rs1386399	0.90[ASN][1000 genomes]
rs1527959	0.90[ASN][1000 genomes]
rs1534418	0.83[ASN][1000 genomes]
rs1534419	0.83[ASN][1000 genomes]
rs1534420	0.83[ASN][1000 genomes]
rs1830260	0.90[ASN][1000 genomes]
rs1843779	0.90[ASN][1000 genomes]
rs1872789	0.84[ASN][1000 genomes]
rs2129509	0.90[ASN][1000 genomes]
rs2204655	0.83[ASN][1000 genomes]
rs2204656	0.84[ASN][1000 genomes]
rs28814605	0.84[ASN][1000 genomes]
rs2901516	0.88[ASN][1000 genomes]
rs4449117	0.82[ASN][1000 genomes]
rs4479415	0.90[ASN][1000 genomes]
rs6545965	0.90[ASN][1000 genomes]
rs6545967	0.88[ASN][1000 genomes]
rs6545968	0.90[ASN][1000 genomes]
rs6705835	0.90[ASN][1000 genomes]
rs6706506	0.90[ASN][1000 genomes]
rs6727888	0.81[ASN][1000 genomes]
rs6734002	0.80[ASN][1000 genomes]
rs6749020	0.90[ASN][1000 genomes]
rs6752010	0.90[ASN][1000 genomes]
rs7349258	0.90[ASN][1000 genomes]
rs7421841	0.84[ASN][1000 genomes]
rs9678363	0.81[ASN][1000 genomes]
rs974344	0.84[ASN][1000 genomes]
rs974345	0.84[ASN][1000 genomes]
rs9751138	0.81[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	nsv535766	chr2:62177655-62929746	Bivalent/Poised TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv916190	chr2:62233785-63006200	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv932487	chr2:62258290-63006200	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv535767	chr2:62461582-63413596	Bivalent Enhancer Strong transcription Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
5	nsv834226	chr2:62745027-62894013	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv874232	chr2:62758044-62906084	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv834237	chr2:62762743-62926036	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:62832200-62868800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:62860800-62861400	Enhancers	HepG2	liver
3	chr2:62861000-62861400	ZNF genes & repeats	Ovary	ovary

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