Variant report

Variant	rs1438017
Chromosome Location	chr2:184349394-184349395
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs4233772	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4233773	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4666913	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4666915	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4666916	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62197582	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62197587	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7567241	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:184342400-184352600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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