Variant report

Variant	rs140377986
Chromosome Location	chr1:172759446-172759447
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3320823	chr1:172759123-172762098	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3320824	chr1:172759183-172762098	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3320825	chr1:172759209-172762035	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3320826	chr1:172759209-172762035	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv16936	chr1:172759326-172761974	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172759000-172760200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr1:172759200-172760000	Enhancers	Placenta Amnion	Placenta Amnion

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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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