Variant report

Variant	rs60751598
Chromosome Location	chr8:64551819-64551820
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs16930569	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16930572	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58364107	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6989408	1.00[ASN][1000 genomes]
rs72649264	1.00[ASN][1000 genomes]
rs72649267	1.00[ASN][1000 genomes]
rs73269092	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7818563	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7818697	0.91[AMR][1000 genomes];1.00[ASN][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	nsv831343	chr8:64436268-64642328	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64545800-64554600	Weak transcription	Fetal Brain Male	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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