Variant report

Variant	rs73207544
Chromosome Location	chr5:108190335-108190336
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs56816112	1.00[AMR][1000 genomes]
rs57038920	1.00[AMR][1000 genomes]
rs57583757	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58369775	1.00[AMR][1000 genomes]
rs59248454	1.00[AMR][1000 genomes]
rs60645247	1.00[AMR][1000 genomes]
rs61246893	1.00[AMR][1000 genomes]
rs73203785	1.00[AMR][1000 genomes]
rs73207509	1.00[AMR][1000 genomes]
rs73207512	1.00[AMR][1000 genomes]
rs73207519	1.00[AMR][1000 genomes]
rs73207522	1.00[AMR][1000 genomes]
rs73207532	1.00[AMR][1000 genomes]
rs73207541	1.00[AMR][1000 genomes]
rs73207542	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73207557	1.00[AMR][1000 genomes]
rs73207559	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73207560	1.00[AMR][1000 genomes]
rs73209319	1.00[AMR][1000 genomes]
rs73209335	1.00[AMR][1000 genomes]
rs73209339	1.00[AMR][1000 genomes]
rs73209350	1.00[AMR][1000 genomes]
rs73209355	1.00[AMR][1000 genomes]
rs73209360	1.00[AMR][1000 genomes]
rs73209361	1.00[AMR][1000 genomes]
rs73209365	1.00[AMR][1000 genomes]
rs73211542	1.00[AMR][1000 genomes]
rs73220148	1.00[AMR][1000 genomes]
rs73220198	1.00[AMR][1000 genomes]
rs73222033	1.00[AMR][1000 genomes]
rs73222038	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882689	chr5:107595383-108299744	Enhancers ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv471039	chr5:108133967-108245089	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv1801555	chr5:108166720-108203055	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:108147000-108198800	Weak transcription	Aorta	Aorta
2	chr5:108147000-108208800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr5:108165800-108194200	Weak transcription	NHEK	skin
4	chr5:108166400-108193600	Weak transcription	Primary B cells from cord blood	blood
5	chr5:108166400-108203200	Weak transcription	HSMM	muscle
6	chr5:108166600-108194600	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr5:108166600-108217000	Weak transcription	Left Ventricle	heart
8	chr5:108167200-108220400	Weak transcription	Fetal Lung	lung
9	chr5:108168200-108194400	Weak transcription	Fetal Heart	heart
10	chr5:108168200-108195000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr5:108168200-108203800	Weak transcription	Adipose Nuclei	Adipose
12	chr5:108169400-108229200	Weak transcription	Fetal Stomach	stomach
13	chr5:108172000-108194000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr5:108173000-108199800	Weak transcription	Brain Angular Gyrus	brain
15	chr5:108173400-108239800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr5:108175400-108194200	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr5:108179000-108193600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr5:108179800-108199800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr5:108179800-108202000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr5:108182000-108217000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr5:108183800-108260400	Weak transcription	Ovary	ovary
22	chr5:108187200-108202600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr5:108187200-108204600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr5:108187200-108211800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr5:108187800-108199200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr5:108188000-108193600	Weak transcription	NHLF	lung
27	chr5:108189600-108190800	Enhancers	Placenta	Placenta
28	chr5:108190200-108190600	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr5:108190200-108192200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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