Variant report

Variant rs16945990
Chromosome Location chr16:48266189-48266190
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:48263400-48268400 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr16:48264400-48269200 Weak transcription Stomach Mucosa stomach
3 chr16:48264600-48270000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr16:48265200-48266600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr16:48265200-48267000 Enhancers HepG2 liver
6 chr16:48265600-48266400 Enhancers NHLF lung
7 chr16:48265600-48266800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr16:48265600-48266800 Enhancers Muscle Satellite Cultured Cells --
9 chr16:48265600-48267000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr16:48265800-48266800 Enhancers NHDF-Ad bronchial
11 chr16:48266000-48266200 Weak transcription Stomach Smooth Muscle stomach
12 chr16:48266000-48266400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr16:48266000-48266600 Weak transcription Liver Liver
14 chr16:48266000-48266800 Enhancers A549 lung
15 chr16:48266000-48266800 Enhancers GM12878-XiMat blood

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