Variant report

Variant	rs4983447
Chromosome Location	chr14:106055056-106055057
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:106049400-106055600	Weak transcription	Pancreas	Pancrea
2	chr14:106049400-106055600	Weak transcription	Spleen	Spleen
3	chr14:106049400-106055800	Weak transcription	Esophagus	oesophagus
4	chr14:106053000-106056000	Enhancers	Placenta	Placenta
5	chr14:106054000-106057000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr14:106054600-106055600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr14:106054800-106055200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr14:106054800-106055800	Enhancers	Colonic Mucosa	Colon
9	chr14:106054800-106056200	Weak transcription	Lung	lung
10	chr14:106055000-106055400	Enhancers	Primary B cells from peripheral blood	blood

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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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