Variant report

Variant	rs62345883
Chromosome Location	chr5:14514799-14514800
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10053327	0.84[EUR][1000 genomes]
rs17500731	0.80[EUR][1000 genomes]
rs17500808	0.91[EUR][1000 genomes]
rs3898746	0.89[EUR][1000 genomes]
rs62345057	0.87[EUR][1000 genomes]
rs62345058	0.87[EUR][1000 genomes]
rs62345059	0.87[EUR][1000 genomes]
rs62345860	1.00[EUR][1000 genomes]
rs62345871	1.00[EUR][1000 genomes]
rs62345872	1.00[EUR][1000 genomes]
rs62345873	1.00[EUR][1000 genomes]
rs62345874	1.00[EUR][1000 genomes]
rs62345875	1.00[EUR][1000 genomes]
rs62345879	1.00[EUR][1000 genomes]
rs62345881	1.00[EUR][1000 genomes]
rs62345882	1.00[EUR][1000 genomes]
rs62345884	0.84[EUR][1000 genomes]
rs62345885	0.84[EUR][1000 genomes]
rs62345886	0.84[EUR][1000 genomes]
rs62345887	0.84[EUR][1000 genomes]
rs6863759	1.00[EUR][1000 genomes]
rs6891562	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026914	chr5:14237782-14751588	Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv1018187	chr5:14385164-15127103	Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	nsv830211	chr5:14474675-14675776	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:14508400-14515400	Weak transcription	Pancreas	Pancrea
2	chr5:14508400-14516400	Weak transcription	Colon Smooth Muscle	Colon
3	chr5:14508800-14515800	Weak transcription	Hela-S3	cervix
4	chr5:14508800-14517200	Weak transcription	Aorta	Aorta
5	chr5:14508800-14520400	Weak transcription	Primary B cells from cord blood	blood
6	chr5:14508800-14525600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr5:14509000-14517000	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr5:14509000-14522000	Weak transcription	Fetal Brain Female	brain
9	chr5:14509200-14523200	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr5:14509400-14515600	Weak transcription	Brain Germinal Matrix	brain
11	chr5:14511200-14517200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr5:14511200-14518000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr5:14511400-14522200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr5:14513800-14519000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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