Variant report

Variant	rs10187410
Chromosome Location	chr2:180268706-180268707
allele	C/T
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]
rs10179699	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10180216	0.90[EUR][1000 genomes]
rs12328936	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13388867	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13403994	0.89[EUR][1000 genomes]
rs13410126	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13415487	0.86[EUR][1000 genomes]
rs13422958	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs60122403	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs60931136	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61258504	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6737562	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72952360	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72962221	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9807927	1.00[CEU][hapmap];0.90[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180267600-180269800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:180268600-180269200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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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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