Variant report

Variant	rs17471449
Chromosome Location	chr9:73479928-73479929
allele	G/T
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	chr9:73427600-73483400	Weak transcription	Aorta	Aorta
2	chr9:73455600-73480600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:73457200-73485200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:73457800-73480600	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr9:73461400-73482000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr9:73466200-73483000	Weak transcription	Fetal Heart	heart
7	chr9:73473600-73481800	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr9:73475600-73481800	Weak transcription	Fetal Kidney	kidney
9	chr9:73478000-73483400	Weak transcription	Ovary	ovary
10	chr9:73478400-73480000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr9:73479400-73480600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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