Variant report

Variant	rs342908
Chromosome Location	chr3:146342377-146342378
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs173144	0.84[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs342905	0.88[ASN][1000 genomes]
rs342906	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs342907	0.99[ASN][1000 genomes]
rs342910	0.94[ASN][1000 genomes]
rs342911	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs342912	0.97[ASN][1000 genomes]
rs342936	0.80[ASN][1000 genomes]
rs342937	0.88[ASN][1000 genomes]
rs342938	0.88[ASN][1000 genomes]
rs342939	0.80[ASN][1000 genomes]
rs342940	0.95[CHB][hapmap]
rs342941	0.95[CHB][hapmap];0.81[JPT][hapmap]
rs343278	0.91[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:146339800-146344000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr3:146340200-146342600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:146340400-146343000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:146341800-146342400	Weak transcription	Dnd41	blood

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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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