Variant report

Variant rs4799583
Chromosome Location chr18:29183587-29183588
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:29179200-29186000 Weak transcription Fetal Intestine Small intestine
2 chr18:29180200-29183800 Weak transcription Liver Liver
3 chr18:29180400-29185600 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr18:29180800-29185400 Weak transcription HepG2 liver
5 chr18:29180800-29191000 Weak transcription Fetal Intestine Large intestine
6 chr18:29182600-29184000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr18:29183000-29183600 Enhancers NHEK skin
8 chr18:29183000-29184000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr18:29183400-29184000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr18:29183400-29184000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --

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