Variant report

Variant	rs2718817
Chromosome Location	chr3:133396671-133396672
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1373551	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1550743	0.80[ASN][1000 genomes]
rs2718804	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2887747	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4241354	0.86[ASN][1000 genomes]
rs4854588	0.86[ASN][1000 genomes]
rs4854739	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6767770	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7623155	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9863253	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133393800-133406800	Weak transcription	Brain Substantia Nigra	brain
2	chr3:133394000-133399600	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr3:133396200-133398800	Weak transcription	HepG2	liver

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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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