Variant report

Variant	rs112218317
Chromosome Location	chr6:28416656-28416657
allele	A/C
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	nsv969368	chr6:28415575-28416789	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:28416200-28417400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
2	chr6:28416200-28417600	Enhancers	Primary T helper cells fromperipheralblood	blood
3	chr6:28416400-28417600	Enhancers	Primary T cells from cord blood	blood
4	chr6:28416400-28417600	Enhancers	Primary T killer memory cells from peripheral blood	blood
5	chr6:28416600-28417000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
6	chr6:28416600-28418000	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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