Variant report

Variant	rs2357321
Chromosome Location	chr2:173018859-173018860
allele	A/C
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	nsv875413	chr2:173009413-173097343	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173017200-173019200	Enhancers	Dnd41	blood
2	chr2:173017600-173019600	Enhancers	Fetal Thymus	thymus
3	chr2:173017600-173020200	Enhancers	Thymus	Thymus
4	chr2:173017800-173019000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr2:173018400-173019000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr2:173018400-173019200	Enhancers	Primary T cells from cord blood	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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