Variant report

Variant	rs376911865
Chromosome Location	chr6:5927753-5927754
allele	C/T
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	esv2333109	chr6:5927555-5927956	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
2	nsv528693	chr6:5927559-5928289	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv993024	chr6:5927748-5927808	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5927400-5928400	Enhancers	NHDF-Ad	bronchial

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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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