Variant report

Variant	rs12306134
Chromosome Location	chr12:118141928-118141929
allele	A/G
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	chr12:118132000-118152400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:118140600-118142400	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr12:118141000-118142200	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr12:118141200-118142200	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr12:118141200-118142400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr12:118141400-118142200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr12:118141400-118142400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr12:118141400-118143200	Enhancers	H1 Cell Line	embryonic stem cell
9	chr12:118141600-118142200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr12:118141600-118142200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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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