Variant report

Variant	rs3026922
Chromosome Location	chr1:159108697-159108698
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11580888	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11582615	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11586482	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2518569	0.86[ASN][1000 genomes]
rs2518570	0.88[ASN][1000 genomes]
rs28620204	0.80[ASN][1000 genomes]
rs3026921	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3026925	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3026935	0.87[CHD][hapmap];0.80[JPT][hapmap];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs41264463	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs59719871	0.84[ASN][1000 genomes]
rs61400225	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs863039	0.83[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:159104400-159110200	Weak transcription	Brain Germinal Matrix	brain

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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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