Variant report

Variant	rs73484065
Chromosome Location	chr13:52933806-52933807
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs56013270	1.00[AMR][1000 genomes]
rs57041737	1.00[AMR][1000 genomes]
rs57313030	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57807149	1.00[AMR][1000 genomes]
rs57855805	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58345586	0.91[AFR][1000 genomes]
rs58452626	1.00[AMR][1000 genomes]
rs60928383	1.00[AMR][1000 genomes]
rs60935342	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61193099	1.00[AMR][1000 genomes]
rs7332023	1.00[AMR][1000 genomes]
rs73484013	1.00[AMR][1000 genomes]
rs73484018	1.00[AMR][1000 genomes]
rs73484032	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73484035	1.00[AMR][1000 genomes]
rs73484037	1.00[AMR][1000 genomes]
rs73484039	1.00[AMR][1000 genomes]
rs73484041	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73484045	0.91[AFR][1000 genomes]
rs73484050	1.00[AMR][1000 genomes]
rs73484052	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73484059	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73484073	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73484080	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73484083	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73484087	1.00[AMR][1000 genomes]
rs73484089	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73484090	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73484102	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73486113	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73486115	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73486116	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73486119	1.00[AMR][1000 genomes]
rs73486122	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73486132	1.00[AMR][1000 genomes]
rs73486157	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73486161	1.00[AMR][1000 genomes]
rs73486169	1.00[AMR][1000 genomes]
rs73486186	1.00[AMR][1000 genomes]
rs73486199	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934070	chr13:52362588-53174923	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
2	nsv1040931	chr13:52564792-53350914	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv541773	chr13:52564792-53350914	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv428288	chr13:52728370-53068132	Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv900084	chr13:52835231-53119704	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	nsv977385	chr13:52918841-52936623	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52931000-52935400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr13:52931200-52935200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr13:52931400-52935200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr13:52931400-52935200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr13:52931400-52935400	Weak transcription	HMEC	breast
6	chr13:52931400-52935400	Weak transcription	NHEK	skin
7	chr13:52931400-52935600	Weak transcription	Osteobl	bone
8	chr13:52931400-52937200	Weak transcription	NH-A	brain
9	chr13:52932800-52934800	Enhancers	Fetal Muscle Leg	muscle
10	chr13:52933200-52934600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr13:52933400-52934200	Enhancers	Liver	Liver
12	chr13:52933400-52934400	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr13:52933600-52934200	Enhancers	HepG2	liver
14	chr13:52933800-52934000	Enhancers	Fetal Intestine Small	intestine
15	chr13:52933800-52934200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr13:52933800-52934200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr13:52933800-52934200	Weak transcription	Fetal Lung	lung
18	chr13:52933800-52934400	Enhancers	NHDF-Ad	bronchial

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