Variant report

Variant	rs12255545
Chromosome Location	chr10:119144795-119144796
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]
rs10437497	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs11197971	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12244521	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12253435	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12262804	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1858553	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs363284	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7907243	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7914137	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7918695	1.00[AMR][1000 genomes]
rs9971320	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:119143000-119146200	Weak transcription	K562	blood
2	chr10:119143200-119147000	Weak transcription	Primary neutrophils fromperipheralblood	blood

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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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