Variant report

Variant	rs60915459
Chromosome Location	chr20:22287786-22287787
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]
rs55906911	1.00[AMR][1000 genomes]
rs55972046	1.00[AMR][1000 genomes]
rs59034302	1.00[AMR][1000 genomes]
rs59545487	1.00[AMR][1000 genomes]
rs73899961	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73899962	1.00[AMR][1000 genomes]
rs73899964	1.00[AMR][1000 genomes]
rs73899965	1.00[AMR][1000 genomes]
rs73899966	1.00[AMR][1000 genomes]
rs73899967	1.00[AMR][1000 genomes]
rs73899994	1.00[AMR][1000 genomes]
rs73900468	1.00[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	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	nsv833942	chr20:22283122-22440749	Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:22286200-22288200	Enhancers	HSMMtube	muscle
2	chr20:22286600-22287800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr20:22286600-22288200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr20:22286600-22288200	Enhancers	NHEK	skin
5	chr20:22286800-22288400	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr20:22287200-22288000	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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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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