Variant report

Variant	rs544913999
Chromosome Location	chr15:62124390-62124391
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	nsv904284	chr15:62123600-62243197	Weak transcription Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:62121800-62126600	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr15:62123000-62124400	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr15:62123400-62124400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr15:62123400-62124600	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr15:62123400-62126400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr15:62124000-62126000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr15:62124200-62126600	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr15:62124200-62127600	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr15:62124200-62127600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

Quick Search:

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

what's new

Quick links