Variant report

Variant	rs73283381
Chromosome Location	chr12:45837739-45837740
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs56404222	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57528325	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60385087	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73283368	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73283376	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73283379	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv972984	chr12:45831852-45839014	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:45827600-45842800	Weak transcription	Aorta	Aorta
2	chr12:45828000-45841800	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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