Variant report

Variant	rs183233780
Chromosome Location	chr4:81509107-81509108
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002776	chr4:81480374-81802614	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv537154	chr4:81480374-81802614	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv9744	chr4:81508721-81509954	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
4	esv3467220	chr4:81508916-81510006	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv3467221	chr4:81508916-81510006	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
6	esv3445528	chr4:81508992-81509909	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:81508400-81509600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr4:81508600-81509400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr4:81508800-81509200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:81508800-81509200	Enhancers	Primary hematopoietic stem cells	blood
5	chr4:81509000-81509200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr4:81509000-81509200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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