Variant report

Variant	rs16903086
Chromosome Location	chr5:36497526-36497527
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36491200-36499800	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr5:36495200-36497600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:36496000-36502200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr5:36496000-36502800	Weak transcription	Stomach Smooth Muscle	stomach
5	chr5:36496200-36501800	Weak transcription	Hela-S3	cervix
6	chr5:36496600-36497600	Enhancers	Brain Hippocampus Middle	brain
7	chr5:36496800-36497800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr5:36497400-36497600	Enhancers	Brain Anterior Caudate	brain

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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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