Variant report

Variant	rs1818483
Chromosome Location	chr3:99320364-99320365
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1618635	0.84[AFR][1000 genomes]
rs1711553	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs485715	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs563041	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs640273	1.00[EUR][1000 genomes]
rs6440724	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6764667	1.00[EUR][1000 genomes]
rs6803793	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs684701	1.00[EUR][1000 genomes]
rs72940133	1.00[EUR][1000 genomes]
rs7652503	0.85[AFR][1000 genomes]
rs9817743	0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530026	chr3:98837320-99340537	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv3422853	chr3:99208019-99342748	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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