Variant report

Variant	rs16963827
Chromosome Location	chr18:30314632-30314633
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:30311000-30322600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr18:30311200-30315400	Weak transcription	NH-A	brain
3	chr18:30311200-30315600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr18:30311200-30321400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr18:30311200-30322800	Weak transcription	Fetal Kidney	kidney
6	chr18:30311400-30315000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr18:30312200-30315600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr18:30312400-30315600	Strong transcription	HepG2	liver
9	chr18:30313600-30315200	Strong transcription	Primary B cells from peripheral blood	blood
10	chr18:30314200-30316000	Strong transcription	Primary B cells from cord blood	blood

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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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