Variant report

Variant	rs146417378
Chromosome Location	chr14:32669287-32669288
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832764	chr14:32564468-32723213	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	esv3380705	chr14:32668101-32670199	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv3527777	chr14:32669175-32761850	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	esv3527778	chr14:32669175-32761850	Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32667600-32670000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:32667600-32670000	Weak transcription	NHEK	skin
3	chr14:32668600-32669800	Weak transcription	Fetal Intestine Small	intestine
4	chr14:32669000-32669600	Enhancers	Primary B cells from cord blood	blood
5	chr14:32669000-32669800	Enhancers	Primary B cells from peripheral blood	blood
6	chr14:32669200-32669400	Enhancers	Primary hematopoietic stem cells	blood
7	chr14:32669200-32669400	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr14:32669200-32669400	Enhancers	GM12878-XiMat	blood
9	chr14:32669200-32669600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr14:32669200-32669800	Enhancers	Liver	Liver
11	chr14:32669200-32669800	Enhancers	Hela-S3	cervix
12	chr14:32669200-32669800	Flanking Active TSS	HepG2	liver
13	chr14:32669200-32669800	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr14:32669200-32670000	Enhancers	Adipose Nuclei	Adipose
15	chr14:32669200-32672400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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