Variant report

Variant	rs56184273
Chromosome Location	chr6:15782300-15782301
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15778600-15784800	Weak transcription	Gastric	stomach
2	chr6:15781600-15782400	Enhancers	Duodenum Mucosa	Duodenum
3	chr6:15781800-15782400	Enhancers	Fetal Intestine Large	intestine
4	chr6:15781800-15782400	Enhancers	Fetal Intestine Small	intestine
5	chr6:15781800-15782400	Enhancers	Stomach Mucosa	stomach
6	chr6:15782000-15782400	Enhancers	Pancreas	Pancrea

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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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