Variant report

Variant	rs6113483
Chromosome Location	chr20:22036524-22036525
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1887056	0.80[ASN][1000 genomes]
rs201585	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs201588	0.85[ASN][1000 genomes]
rs201589	0.80[ASN][1000 genomes]
rs201590	0.85[ASN][1000 genomes]
rs201592	0.85[ASN][1000 genomes]
rs201593	0.86[ASN][1000 genomes]
rs201594	0.87[ASN][1000 genomes]
rs2876631	0.87[ASN][1000 genomes]
rs4813446	0.80[ASN][1000 genomes]
rs4815090	0.81[EUR][1000 genomes]
rs6036026	0.80[ASN][1000 genomes]
rs6036027	0.80[ASN][1000 genomes]
rs6036029	0.80[ASN][1000 genomes]
rs6047844	0.87[ASN][1000 genomes]
rs6113495	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6113496	0.80[ASN][1000 genomes]
rs6132477	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6137527	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][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	nsv1058137	chr20:21549350-22295051	Weak transcription Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv432114	chr20:22012900-22148200	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 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	chr20:22029200-22038000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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