Variant report

Variant	rs9789776
Chromosome Location	chr2:180519313-180519314
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10174391	0.87[AFR][1000 genomes]
rs10178119	0.87[AFR][1000 genomes]
rs10201428	0.87[AFR][1000 genomes]
rs10497545	0.94[AFR][1000 genomes]
rs10930882	0.93[ASN][1000 genomes]
rs11690551	0.96[ASN][1000 genomes]
rs1399689	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1515292	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1877944	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2203462	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4893879	0.94[AFR][1000 genomes]
rs71405993	0.88[AFR][1000 genomes]
rs72958961	0.93[ASN][1000 genomes]
rs932117	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs952507	0.94[AFR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180517400-180521400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:180518400-180519400	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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