Variant report

Variant	rs73457645
Chromosome Location	chr7:136320966-136320967
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs58692102	1.00[AMR][1000 genomes]
rs59103221	1.00[AMR][1000 genomes]
rs59580970	1.00[AMR][1000 genomes]
rs61093667	1.00[AMR][1000 genomes]
rs73443517	1.00[AMR][1000 genomes]
rs73443599	1.00[AMR][1000 genomes]
rs73459634	1.00[AMR][1000 genomes]
rs73459657	1.00[AMR][1000 genomes]
rs73459662	1.00[AMR][1000 genomes]
rs73459663	1.00[AMR][1000 genomes]
rs73459665	1.00[AMR][1000 genomes]
rs73459667	1.00[AMR][1000 genomes]
rs73459677	1.00[AMR][1000 genomes]
rs73459684	1.00[AMR][1000 genomes]
rs73459697	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	nsv518439	chr7:136134265-136452082	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr7:136319600-136323400	Enhancers	Fetal Brain Male	brain
2	chr7:136320600-136322400	Enhancers	Fetal Brain Female	brain

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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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