Variant report

Variant	rs73583882
Chromosome Location	chr16:80135305-80135306
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs16952472	0.87[AFR][1000 genomes]
rs2126998	1.00[AFR][1000 genomes]
rs4889097	1.00[AFR][1000 genomes]
rs57189314	0.92[AFR][1000 genomes]
rs57824584	0.92[AFR][1000 genomes]
rs57899846	0.92[AFR][1000 genomes]
rs57929477	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73583891	0.83[AMR][1000 genomes]
rs73583892	0.83[AMR][1000 genomes]
rs73585959	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73585965	0.83[AMR][1000 genomes]
rs73587910	0.90[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv906995	chr16:80094975-80166677	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv833298	chr16:80122337-80314603	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80127000-80137200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr16:80134400-80136200	Enhancers	HMEC	breast
3	chr16:80134400-80137400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr16:80134400-80137400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr16:80134800-80138600	Weak transcription	Osteobl	bone
6	chr16:80135000-80138600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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Input of quick search could be:

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

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