Variant report

Variant	rs73063843
Chromosome Location	chr3:34970889-34970890
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11925888	0.91[ASN][1000 genomes]
rs12053892	0.95[ASN][1000 genomes]
rs12632359	0.86[ASN][1000 genomes]
rs1357428	0.82[ASN][1000 genomes]
rs1474299	0.96[ASN][1000 genomes]
rs17032340	0.87[ASN][1000 genomes]
rs17032385	0.93[ASN][1000 genomes]
rs2071488	0.85[ASN][1000 genomes]
rs4549234	0.87[ASN][1000 genomes]
rs4575830	0.96[ASN][1000 genomes]
rs4678716	0.87[ASN][1000 genomes]
rs4678717	0.90[ASN][1000 genomes]
rs4678724	0.97[ASN][1000 genomes]
rs56235912	0.94[ASN][1000 genomes]
rs58778451	0.83[ASN][1000 genomes]
rs59750319	0.83[ASN][1000 genomes]
rs62260224	0.96[ASN][1000 genomes]
rs6550306	0.82[ASN][1000 genomes]
rs6792813	0.87[ASN][1000 genomes]
rs73061969	0.93[ASN][1000 genomes]
rs73063864	0.91[ASN][1000 genomes]
rs7650825	0.84[ASN][1000 genomes]
rs7653203	0.91[ASN][1000 genomes]
rs940047	0.84[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	nsv876686	chr3:34967346-35075355	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:34970200-34971200	Enhancers	Cortex derived primary cultured neurospheres	brain

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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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