Variant report

Variant	rs73575840
Chromosome Location	chr16:80075811-80075812
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs58944962	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73571906	1.00[AMR][1000 genomes]
rs73573909	1.00[AMR][1000 genomes]
rs73573930	1.00[AMR][1000 genomes]
rs73573932	1.00[AMR][1000 genomes]
rs73573935	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73573938	1.00[AMR][1000 genomes]
rs73574002	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73575815	1.00[AMR][1000 genomes]
rs73575816	1.00[AMR][1000 genomes]
rs73575832	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73575834	1.00[AMR][1000 genomes]
rs73575837	1.00[AMR][1000 genomes]
rs73575842	1.00[AMR][1000 genomes]
rs73575850	1.00[AMR][1000 genomes]
rs73583878	1.00[AMR][1000 genomes]
rs73585968	1.00[AMR][1000 genomes]
rs73585997	1.00[AMR][1000 genomes]
rs73589924	1.00[AMR][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	nsv573285	chr16:79158182-80127326	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv573294	chr16:80005642-80131944	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80072200-80076000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr16:80072800-80085200	Weak transcription	Esophagus	oesophagus
3	chr16:80073200-80078000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr16:80074200-80076000	Enhancers	NHEK	skin
5	chr16:80074200-80076800	Enhancers	Placenta Amnion	Placenta Amnion
6	chr16:80074400-80076400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr16:80075000-80079600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr16:80075400-80076000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr16:80075400-80076200	Enhancers	Small Intestine	intestine
10	chr16:80075600-80076000	Enhancers	Fetal Intestine Large	intestine
11	chr16:80075800-80076000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr16:80075800-80077400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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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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