Variant report

Variant	rs6780730
Chromosome Location	chr3:118230867-118230868
allele	C/T
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:11)

rs_ID	r²[population]
rs1554385	1.00[ASN][1000 genomes]
rs16828633	0.88[EUR][1000 genomes]
rs16828635	0.89[EUR][1000 genomes]
rs4131580	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4131581	0.89[EUR][1000 genomes]
rs4383519	0.86[EUR][1000 genomes]
rs62275962	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62275963	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6800781	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7625296	0.89[EUR][1000 genomes]
rs939316	0.80[AMR][1000 genomes];0.96[EUR][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	nsv829690	chr3:118205361-118378010	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr3:118227600-118231600	Weak transcription	Fetal Lung	lung

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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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