Variant report

Variant	rs17001751
Chromosome Location	chr4:77212925-77212926
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:77173800-77215800	Weak transcription	Brain Hippocampus Middle	brain
2	chr4:77186600-77215000	Weak transcription	Brain Anterior Caudate	brain
3	chr4:77194200-77216400	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr4:77202400-77217000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr4:77202400-77221000	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr4:77203000-77214600	Weak transcription	Adipose Nuclei	Adipose
7	chr4:77204400-77213400	Weak transcription	Liver	Liver
8	chr4:77204600-77214400	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr4:77205400-77213800	Weak transcription	Pancreas	Pancrea
10	chr4:77209200-77213800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr4:77212000-77218000	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr4:77212400-77219400	Weak transcription	Fetal Intestine Small	intestine
13	chr4:77212600-77213800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:77212600-77215800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr4:77212600-77217400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr4:77212600-77227000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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