Variant report

Variant	rs4983371
Chromosome Location	chr14:106107974-106107975
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs2104053	0.87[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	nsv530813	chr14:105607701-106453697	Strong transcription Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	149 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:106105600-106108200	Enhancers	Liver	Liver
2	chr14:106106600-106112200	Weak transcription	Spleen	Spleen
3	chr14:106106800-106108000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr14:106106800-106108000	Enhancers	Stomach Smooth Muscle	stomach
5	chr14:106106800-106108200	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr14:106106800-106108200	Strong transcription	Primary B cells from peripheral blood	blood
7	chr14:106106800-106108200	Enhancers	Lung	lung
8	chr14:106107400-106108200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr14:106107600-106108000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr14:106107800-106112600	Weak transcription	Gastric	stomach
11	chr14:106107800-106116800	Weak transcription	Pancreas	Pancrea

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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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