Variant report

Variant	rs73532279
Chromosome Location	chr13:85220999-85221000
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs17078491	0.83[AMR][1000 genomes]
rs73532263	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73532284	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9565952	0.83[AFR][1000 genomes]
rs9669930	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	nsv949402	chr13:84675752-85606846	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv456046	chr13:84971270-85262508	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv562561	chr13:84971270-85262508	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv900691	chr13:85206473-85294881	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv1851778	chr13:85206473-85299207	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv900692	chr13:85218788-85294881	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:85218600-85222400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr13:85219200-85225200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr13:85219800-85227600	Weak transcription	Right Ventricle	heart
4	chr13:85219800-85229800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr13:85220000-85221000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr13:85220000-85224000	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr13:85220000-85224000	Weak transcription	NHEK	skin
8	chr13:85220000-85225400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr13:85220200-85223800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr13:85220200-85224000	Weak transcription	NH-A	brain
11	chr13:85220200-85225600	Weak transcription	Left Ventricle	heart
12	chr13:85220400-85228200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr13:85220600-85221000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr13:85220600-85221000	Weak transcription	Osteobl	bone
15	chr13:85220800-85221400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr13:85220800-85221400	Enhancers	Primary hematopoietic stem cells	blood
17	chr13:85220800-85221600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr13:85220800-85221600	Enhancers	Fetal Heart	heart
19	chr13:85220800-85221800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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