Variant report

Variant	rs55859033
Chromosome Location	chr10:93289604-93289605
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93272200-93296000	Weak transcription	HSMMtube	muscle
2	chr10:93278200-93296000	Weak transcription	HSMM	muscle
3	chr10:93278400-93298400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr10:93288000-93290000	Enhancers	Pancreas	Pancrea
5	chr10:93288400-93290000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
6	chr10:93288600-93296000	Weak transcription	Right Atrium	heart
7	chr10:93289200-93290800	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr10:93289400-93296000	Weak transcription	Liver	Liver
9	chr10:93289600-93296000	Weak transcription	Aorta	Aorta

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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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