Variant report

Variant	rs58097245
Chromosome Location	chr20:24105450-24105451
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12106019	1.00[AMR][1000 genomes]
rs12106188	1.00[AMR][1000 genomes]
rs13433317	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1884518	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2224231	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59960570	0.97[AFR][1000 genomes]
rs60507886	0.84[AFR][1000 genomes]
rs60840217	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6106789	0.84[AFR][1000 genomes]
rs6114480	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8117417	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	nsv9793	chr20:23939613-24734850	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	esv3328348	chr20:24095746-24285830	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	7 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	chr20:24104200-24109600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:24104400-24106000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr20:24104600-24111600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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