Variant report

Variant	rs569508332
Chromosome Location	chr1:172786867-172786868
allele	A/G
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	nsv947450	chr1:172786009-172789082	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172785400-172788400	Weak transcription	HSMMtube	muscle
2	chr1:172786400-172789400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr1:172786600-172788000	Enhancers	Primary B cells from cord blood	blood
4	chr1:172786600-172788400	Enhancers	Primary B cells from peripheral blood	blood
5	chr1:172786800-172788000	Flanking Active TSS	GM12878-XiMat	blood
6	chr1:172786800-172788200	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr1:172786800-172789400	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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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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