Variant report

Variant	rs550963976
Chromosome Location	chr3:82074755-82074756
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007167	chr3:82050178-82301466	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv877041	chr3:82074024-82363196	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:82073600-82080000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:82073800-82075000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr3:82074000-82074800	Active TSS	Primary B cells from cord blood	blood
4	chr3:82074600-82074800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr3:82074600-82075000	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr3:82074600-82075000	Enhancers	Primary B cells from peripheral blood	blood
7	chr3:82074600-82075000	Enhancers	Ovary	ovary
8	chr3:82074600-82075000	Enhancers	Monocytes-CD14+_RO01746	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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