Variant report

Variant	rs73409526
Chromosome Location	chr12:117771155-117771156
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117728000-117771200	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr12:117739800-117771400	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr12:117762200-117771200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr12:117765000-117773000	Weak transcription	Pancreas	Pancrea
5	chr12:117770200-117772800	Weak transcription	NHEK	skin
6	chr12:117770800-117771400	Bivalent Enhancer	Fetal Brain Male	brain
7	chr12:117770800-117771600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr12:117770800-117771600	Enhancers	A549	lung
9	chr12:117771000-117771200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr12:117771000-117771200	Active TSS	Fetal Brain Female	brain
11	chr12:117771000-117771400	Bivalent Enhancer	Brain Germinal Matrix	brain
12	chr12:117771000-117771400	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
13	chr12:117771000-117772000	Enhancers	H1 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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