Variant report

Variant	rs12035448
Chromosome Location	chr1:225050082-225050083
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10753397	0.94[ASN][1000 genomes]
rs10915727	0.92[ASN][1000 genomes]
rs10915728	0.91[ASN][1000 genomes]
rs11579084	0.82[ASN][1000 genomes]
rs12028207	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12404833	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1857623	0.87[ASN][1000 genomes]
rs1892123	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2263439	0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2405780	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59060615	0.92[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:225049200-225051200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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