Variant report

Variant	rs61939864
Chromosome Location	chr12:118253010-118253011
allele	A/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]
rs1078653	0.85[AMR][1000 genomes]
rs11068675	0.85[AMR][1000 genomes]
rs11832804	0.80[AMR][1000 genomes]
rs17585881	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35724007	0.80[AMR][1000 genomes]
rs4547183	0.97[EUR][1000 genomes]
rs56296939	0.85[AMR][1000 genomes]
rs56918257	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61937746	0.80[AMR][1000 genomes]
rs61939860	0.97[EUR][1000 genomes]
rs61939862	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6490153	0.81[AMR][1000 genomes]
rs6490155	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7309450	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7960031	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118237200-118254000	Weak transcription	iPS DF 19.11 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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