Variant report

Variant	rs539461172
Chromosome Location	chr8:49859816-49859817
allele	C/T
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	esv3328866	chr8:49858699-49862897	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49859000-49860200	Weak transcription	Liver	Liver
2	chr8:49859400-49860000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr8:49859600-49860000	Enhancers	Primary T cells fromperipheralblood	blood
4	chr8:49859600-49860800	Weak transcription	Fetal Brain Male	brain
5	chr8:49859800-49865000	Enhancers	Primary T helper naive cells from peripheral 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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