Variant report

Variant	rs10979153
Chromosome Location	chr9:110747860-110747861
allele	A/G
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	chr9:110746000-110751200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr9:110746200-110750000	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr9:110746200-110751200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr9:110746200-110751200	Weak transcription	NHDF-Ad	bronchial
5	chr9:110746400-110751000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr9:110746600-110748000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr9:110747000-110749600	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr9:110747200-110749600	Weak transcription	Primary monocytes 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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