Variant report

Variant	rs16988948
Chromosome Location	chr19:51655847-51655848
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51650400-51677000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:51654400-51659800	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr19:51654400-51661200	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr19:51655200-51658800	Strong transcription	Primary neutrophils fromperipheralblood	blood
5	chr19:51655600-51656600	Weak transcription	Spleen	Spleen
6	chr19:51655600-51660800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr19:51655800-51659000	Strong transcription	Primary mononuclear 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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