Variant report

Variant rs55830747
Chromosome Location chr13:48870968-48870969
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:48844400-48877200 Weak transcription Aorta Aorta
2 chr13:48863000-48876400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
3 chr13:48866200-48876800 Weak transcription Pancreas Pancrea
4 chr13:48866200-48877200 Weak transcription Left Ventricle heart
5 chr13:48866600-48876600 Weak transcription Skeletal Muscle Female skeletal muscle
6 chr13:48868000-48876800 Weak transcription Stomach Mucosa stomach
7 chr13:48868200-48871000 Weak transcription HepG2 liver
8 chr13:48869800-48872200 Enhancers Fetal Thymus thymus
9 chr13:48870200-48871200 Strong transcription Breast Myoepithelial Primary Cells Breast
10 chr13:48870200-48877000 Weak transcription HSMMtube muscle
11 chr13:48870400-48871000 Enhancers Primary B cells from peripheral blood blood
12 chr13:48870400-48871600 Enhancers Dnd41 blood
13 chr13:48870600-48871800 Enhancers Placenta Amnion Placenta Amnion
14 chr13:48870600-48872000 Enhancers Thymus Thymus
15 chr13:48870800-48871000 Enhancers Primary hematopoietic stem cells short term culture blood

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