Variant report

Variant	rs73323985
Chromosome Location	chr10:93462133-93462134
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs56001634	1.00[AMR][1000 genomes]
rs56035629	1.00[AMR][1000 genomes]
rs56078226	1.00[AMR][1000 genomes]
rs56214670	1.00[AMR][1000 genomes]
rs56226527	1.00[AMR][1000 genomes]
rs56327910	1.00[AMR][1000 genomes]
rs56358636	1.00[AMR][1000 genomes]
rs56367452	1.00[AMR][1000 genomes]
rs56684777	1.00[AMR][1000 genomes]
rs57058393	1.00[AMR][1000 genomes]
rs57095232	1.00[AMR][1000 genomes]
rs58926566	1.00[AMR][1000 genomes]
rs59026711	1.00[AMR][1000 genomes]
rs61218533	1.00[AMR][1000 genomes]
rs73312343	1.00[AMR][1000 genomes]
rs74149282	1.00[AMR][1000 genomes]
rs74149289	1.00[AMR][1000 genomes]
rs74149292	1.00[AMR][1000 genomes]
rs74149303	1.00[AMR][1000 genomes]
rs74149304	1.00[AMR][1000 genomes]
rs74149306	1.00[AMR][1000 genomes]
rs74149308	1.00[AMR][1000 genomes]
rs74149309	1.00[AMR][1000 genomes]
rs74149310	1.00[AMR][1000 genomes]
rs74151715	1.00[AMR][1000 genomes]
rs74151717	1.00[AMR][1000 genomes]
rs74151727	1.00[AMR][1000 genomes]
rs74151730	1.00[AMR][1000 genomes]
rs74151733	1.00[AMR][1000 genomes]
rs74151738	1.00[AMR][1000 genomes]
rs74151739	1.00[AMR][1000 genomes]
rs74151743	1.00[AMR][1000 genomes]
rs74151744	1.00[AMR][1000 genomes]
rs74151745	1.00[AMR][1000 genomes]
rs74151748	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895892	chr10:93432632-93470167	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93461200-93462400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:93461200-93463200	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr10:93461400-93466000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr10:93461600-93467200	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr10:93461600-93467200	Weak transcription	Hela-S3	cervix
6	chr10:93461600-93468000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr10:93462000-93462800	Enhancers	Liver	Liver
8	chr10:93462000-93462800	Enhancers	K562	blood

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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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