Variant report

Variant	rs342938
Chromosome Location	chr3:146350346-146350347
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs173144	0.92[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs342905	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs342906	0.88[ASN][1000 genomes]
rs342907	0.87[ASN][1000 genomes]
rs342908	0.88[ASN][1000 genomes]
rs342910	0.82[ASN][1000 genomes]
rs342911	0.87[ASN][1000 genomes]
rs342912	0.85[ASN][1000 genomes]
rs342934	0.89[ASN][1000 genomes]
rs342935	0.87[ASN][1000 genomes]
rs342936	0.92[ASN][1000 genomes]
rs342937	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs342939	0.92[ASN][1000 genomes]
rs342940	1.00[CHB][hapmap];0.93[CHD][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs342941	1.00[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs343278	0.80[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:146344600-146351000	Weak transcription	Colon Smooth Muscle	Colon
2	chr3:146346000-146350800	Weak transcription	HepG2	liver
3	chr3:146350200-146351000	Enhancers	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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