Variant report

Variant	rs73060667
Chromosome Location	chr3:34638097-34638098
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11129600	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34234856	0.83[ASN][1000 genomes]
rs6773245	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6788571	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6790851	0.88[ASN][1000 genomes]
rs73060691	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9311059	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9881586	0.80[ASN][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	nsv876685	chr3:34615754-34662157	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:34637400-34638600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:34637600-34638800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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