Variant report

Variant	rs9904202
Chromosome Location	chr17:34214991-34214992
allele	A/C/T
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	chr17:34192200-34218000	Weak transcription	Stomach Smooth Muscle	stomach
2	chr17:34207400-34219200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr17:34208000-34215800	Weak transcription	Placenta	Placenta
4	chr17:34208400-34215200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr17:34208400-34215400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr17:34208600-34215400	Weak transcription	GM12878-XiMat	blood
7	chr17:34214200-34223000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr17:34214600-34216200	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr17:34214800-34221800	Enhancers	Primary T 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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