Variant report

Variant	rs12247343
Chromosome Location	chr10:22730392-22730393
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:22726800-22731400	Weak transcription	Gastric	stomach
2	chr10:22727400-22732600	Weak transcription	HSMM	muscle
3	chr10:22727600-22732000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr10:22727800-22733000	Weak transcription	Osteobl	bone
5	chr10:22728000-22730600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr10:22728000-22731400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr10:22728000-22731800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr10:22728000-22732600	Weak transcription	GM12878-XiMat	blood
9	chr10:22728000-22732600	Weak transcription	HSMMtube	muscle
10	chr10:22728000-22733200	Weak transcription	Stomach Mucosa	stomach
11	chr10:22728000-22734200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr10:22728200-22732200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr10:22728200-22732200	Weak transcription	Primary B cells from peripheral blood	blood
14	chr10:22730000-22732000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr10:22730200-22731000	Enhancers	K562	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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