Variant report

Variant	rs2424563
Chromosome Location	chr20:23598355-23598356
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10485646	0.82[ASN][1000 genomes]
rs2983639	0.80[ASN][1000 genomes]
rs3004148	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs35701829	0.80[ASN][1000 genomes]
rs6106689	0.81[ASN][1000 genomes]
rs6106691	0.82[ASN][1000 genomes]
rs62207039	0.80[ASN][1000 genomes]
rs62208864	0.81[ASN][1000 genomes]
rs7265919	0.82[ASN][1000 genomes]
rs8120131	0.82[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	nsv491876	chr20:23436633-24031374	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23595200-23601600	Weak transcription	Lung	lung
2	chr20:23595200-23603400	Weak transcription	Brain Anterior Caudate	brain
3	chr20:23598200-23603000	Weak transcription	Primary monocytes fromperipheralblood	blood

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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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