Variant report

Variant	rs9697123
Chromosome Location	chr9:110729635-110729636
allele	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	chr9:110724200-110730200	Weak transcription	Stomach Mucosa	stomach
2	chr9:110726800-110738400	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr9:110727000-110738200	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr9:110727600-110732200	Weak transcription	Gastric	stomach
5	chr9:110728800-110730200	Enhancers	Brain Cingulate Gyrus	brain
6	chr9:110729000-110730600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr9:110729200-110730200	Weak transcription	Brain Hippocampus Middle	brain
8	chr9:110729400-110729800	Weak transcription	Esophagus	oesophagus
9	chr9:110729600-110730000	Enhancers	Primary neutrophils fromperipheralblood	blood

Quick Search:

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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