Variant report

Variant rs16830593
Chromosome Location chr2:152873088-152873089
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:152867800-152881800 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr2:152872000-152873200 Enhancers Fetal Brain Male brain
3 chr2:152872000-152873400 Bivalent Enhancer Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr2:152872000-152873800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
5 chr2:152872000-152873800 Enhancers Cortex derived primary cultured neurospheres brain
6 chr2:152872200-152873400 Enhancers Brain Germinal Matrix brain
7 chr2:152872200-152873600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr2:152872200-152873800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
9 chr2:152872400-152873600 Enhancers Fetal Brain Female brain
10 chr2:152872400-152882200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr2:152872800-152873400 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr2:152873000-152873400 Flanking Active TSS HepG2 liver

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