Variant report

Variant	rs537496073
Chromosome Location	chr20:22452463-22452464
allele	G/T
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	esv3428094	chr20:22450900-22453266	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:22451200-22452800	Enhancers	Stomach Mucosa	stomach
2	chr20:22451600-22452600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr20:22451600-22452800	Enhancers	Gastric	stomach
4	chr20:22452000-22452800	Enhancers	Pancreas	Pancrea
5	chr20:22452200-22452800	Enhancers	K562	blood
6	chr20:22452200-22453200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr20:22452400-22452600	Flanking Active TSS	HepG2	liver
8	chr20:22452400-22453200	Enhancers	A549	lung
9	chr20:22452400-22453400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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