Variant report

Variant	rs12268922
Chromosome Location	chr10:117641458-117641459
allele	A/G
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	chr10:117634000-117657800	Weak transcription	Aorta	Aorta
2	chr10:117636800-117644000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr10:117639800-117642600	Weak transcription	Fetal Stomach	stomach
4	chr10:117641200-117641600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr10:117641200-117642000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
6	chr10:117641200-117642200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
7	chr10:117641400-117641600	Enhancers	H9 Cell Line	embryonic stem cell
8	chr10:117641400-117641600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
9	chr10:117641400-117641800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
10	chr10:117641400-117641800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
11	chr10:117641400-117641800	Enhancers	iPS DF 6.9 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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