Variant report

Variant	rs34738779
Chromosome Location	chr7:103633511-103633512
allele	AG/TA
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs12540614	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4305831	0.90[EUR][1000 genomes]
rs4727584	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4729943	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62488860	0.90[EUR][1000 genomes]
rs6465952	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67196278	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6949973	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6967863	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6972426	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6975845	0.84[EUR][1000 genomes]
rs7800855	0.90[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103631600-103636200	Enhancers	K562	blood
2	chr7:103632800-103633800	Weak transcription	HepG2	liver

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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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