Variant report

Variant	rs977220
Chromosome Location	chr2:115795056-115795057
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10164698	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10175592	1.00[AMR][1000 genomes]
rs12711814	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12711815	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1396935	1.00[AMR][1000 genomes]
rs1848756	1.00[AMR][1000 genomes]
rs1980005	1.00[AMR][1000 genomes]
rs1980006	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2136543	1.00[AMR][1000 genomes]
rs4849376	0.80[AFR][1000 genomes]
rs6542234	1.00[AMR][1000 genomes]
rs6755919	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7593027	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8179805	1.00[AMR][1000 genomes]
rs9308705	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs966821	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs977221	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	chr2:115793800-115795200	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr2:115794400-115795200	Enhancers	iPS-18 Cell Line	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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