Variant report

Variant	rs190218126
Chromosome Location	chr3:151426357-151426358
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

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	nsv995048	chr3:151114074-151560019	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	esv3449164	chr3:151425303-151453439	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv966962	chr3:151425308-151446146	Enhancers ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:151424800-151427800	Enhancers	NH-A	brain
2	chr3:151425600-151427000	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr3:151425800-151427000	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr3:151425800-151427600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr3:151426000-151426600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr3:151426000-151427000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr3:151426200-151426600	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr3:151426200-151427000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr3:151426200-151427000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:151426200-151427000	Enhancers	HUES64 Cell Line	embryonic stem cell

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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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