Variant report

Variant	rs60195382
Chromosome Location	chr1:211392465-211392466
allele	-/CT
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3340221	chr1:211391629-211393677	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv3337898	chr1:211392229-211393277	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv155432	chr1:211392465-211392468	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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