Variant report

Variant	rs56967546
Chromosome Location	chr18:30306542-30306543
allele	A/G
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]
rs11873545	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11873557	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16963733	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16963826	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2004848	1.00[AMR][1000 genomes]
rs57955315	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59546539	0.95[AFR][1000 genomes]
rs59987102	0.95[AFR][1000 genomes]
rs73411249	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73411257	0.84[AFR][1000 genomes]
rs7342998	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8092034	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:30294800-30306800	Weak transcription	Primary B cells from peripheral blood	blood
2	chr18:30301200-30307800	Weak transcription	HepG2	liver
3	chr18:30305600-30307000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr18:30305600-30310000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr18:30305800-30308400	Weak transcription	Primary B cells from cord blood	blood

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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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