Variant report

Variant	rs12246226
Chromosome Location	chr10:18594002-18594003
allele	A/T
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	chr10:18574600-18601400	Weak transcription	Fetal Lung	lung
2	chr10:18579200-18603400	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr10:18592200-18596200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr10:18593200-18602200	Weak transcription	Pancreas	Pancrea
5	chr10:18593400-18594600	Enhancers	Primary hematopoietic stem cells	blood
6	chr10:18593400-18597400	Weak transcription	Rectal Smooth Muscle	rectum
7	chr10:18593600-18595000	Weak transcription	Ovary	ovary
8	chr10:18593600-18597200	Weak transcription	Fetal Heart	heart
9	chr10:18593600-18599400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr10:18593800-18595600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr10:18593800-18597200	Weak transcription	Stomach Smooth Muscle	stomach
12	chr10:18594000-18594400	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr10:18594000-18595400	Enhancers	Monocytes-CD14+_RO01746	blood

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

what's new

Quick links