Variant report

Variant	rs594168
Chromosome Location	chr12:123169056-123169057
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123164200-123171600	Weak transcription	Esophagus	oesophagus
2	chr12:123164200-123171800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr12:123166600-123175400	Weak transcription	Adipose Nuclei	Adipose
4	chr12:123166600-123187800	Weak transcription	A549	lung
5	chr12:123168600-123169400	Enhancers	HepG2	liver
6	chr12:123168800-123169600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr12:123168800-123169600	Enhancers	Liver	Liver

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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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