Variant report

Variant	rs6790525
Chromosome Location	chr3:18098694-18098695
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1355724	0.96[ASN][1000 genomes]
rs2203242	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34590963	1.00[EUR][1000 genomes]
rs4132218	0.96[EUR][1000 genomes]
rs4688898	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4688899	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4688913	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7627583	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7645289	0.95[EUR][1000 genomes]
rs9857811	0.95[EUR][1000 genomes]
rs9859212	1.00[EUR][1000 genomes]
rs9861146	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:18086800-18113400	Weak transcription	Fetal Thymus	thymus
2	chr3:18098000-18102000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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