Variant report

Variant	rs11265941
Chromosome Location	chr9:92471176-92471177
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:92465800-92507200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:92467800-92477800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr9:92469200-92472400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr9:92469600-92474600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr9:92469800-92476000	Weak transcription	Fetal Lung	lung
6	chr9:92470400-92471800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr9:92470400-92472000	Weak transcription	Adipose Nuclei	Adipose
8	chr9:92470400-92472000	Weak transcription	Right Ventricle	heart
9	chr9:92470400-92472400	Weak transcription	Right Atrium	heart
10	chr9:92470600-92472000	Weak transcription	Fetal Muscle Leg	muscle
11	chr9:92470600-92472000	Weak transcription	Placenta	Placenta

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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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