Variant report

Variant	rs58036995
Chromosome Location	chr20:10777062-10777063
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs16991987	1.00[AMR][1000 genomes]
rs56348465	1.00[AMR][1000 genomes]
rs58565167	1.00[AMR][1000 genomes]
rs6032968	1.00[AMR][1000 genomes]
rs6040190	1.00[AMR][1000 genomes]
rs6040193	1.00[AMR][1000 genomes]
rs7261930	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7265005	1.00[AMR][1000 genomes]
rs7274741	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73896403	1.00[AMR][1000 genomes]
rs73898834	1.00[AMR][1000 genomes]
rs73898836	1.00[AMR][1000 genomes]
rs73898841	1.00[AMR][1000 genomes]
rs73898852	1.00[AMR][1000 genomes]
rs73898854	1.00[AMR][1000 genomes]
rs73898858	1.00[AMR][1000 genomes]
rs73898860	1.00[AMR][1000 genomes]
rs73898863	1.00[AMR][1000 genomes]
rs73898864	1.00[AMR][1000 genomes]
rs73898866	1.00[AMR][1000 genomes]
rs73898870	1.00[AMR][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	nsv522874	chr20:9899439-10819210	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:10771200-10779400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr20:10771200-10779600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr20:10773400-10779400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr20:10773600-10781200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr20:10775400-10787200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr20:10775600-10787800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr20:10776600-10777800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr20:10777000-10777400	Weak transcription	Pancreas	Pancrea
9	chr20:10777000-10780400	Weak transcription	Stomach Mucosa	stomach

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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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