Variant report

Variant	rs6490157
Chromosome Location	chr12:118251526-118251527
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10774960	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1374249	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2121299	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4766878	0.85[ASN][1000 genomes]
rs4766879	0.85[ASN][1000 genomes]
rs4767626	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6490156	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7297777	0.90[EUR][1000 genomes]
rs7297790	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7979661	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]

No data

Chromatin state (count:2 , 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
2	chr12:118248400-118252200	Weak transcription	Placenta Amnion	Placenta Amnion

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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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