Variant report

Variant	rs6559655
Chromosome Location	chr9:72234954-72234955
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72215600-72235200	Weak transcription	Aorta	Aorta
2	chr9:72219800-72242600	Weak transcription	Left Ventricle	heart
3	chr9:72221200-72237200	Weak transcription	Ovary	ovary
4	chr9:72226200-72236800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr9:72232200-72239800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr9:72233600-72237400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr9:72234000-72236800	Weak transcription	Brain Anterior Caudate	brain
8	chr9:72234000-72237200	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr9:72234000-72237200	Weak transcription	Fetal Stomach	stomach
10	chr9:72234200-72237200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr9:72234800-72236400	Strong transcription	Liver	Liver
12	chr9:72234800-72237200	Weak transcription	Brain Substantia Nigra	brain
13	chr9:72234800-72237800	Weak transcription	Fetal Kidney	kidney

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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