Variant report

Variant	rs58999525
Chromosome Location	chr12:118264454-118264455
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118253800-118266400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr12:118256600-118266400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr12:118257200-118266400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr12:118264200-118266400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:118264400-118264600	Enhancers	Placenta Amnion	Placenta Amnion
6	chr12:118264400-118265400	Weak transcription	Dnd41	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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