Variant report

Variant	rs539078282
Chromosome Location	chr10:25035167-25035168
allele	A/T
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	esv2181761	chr10:25035024-25035455	Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
2	esv3480840	chr10:25035054-25035324	Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
3	esv3399462	chr10:25035082-25035380	Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
4	esv3424745	chr10:25035084-25035405	Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
5	esv3455	chr10:25035139-25035357	Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
6	esv3435891	chr10:25035154-25035308	Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25034600-25035200	Active TSS	Placenta	Placenta
2	chr10:25035000-25035200	Active TSS	HepG2	liver
3	chr10:25035000-25035600	Active TSS	A549	lung

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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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