Variant report

Variant rs1449220
Chromosome Location chr16:77718362-77718363
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:77716600-77719000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
2 chr16:77717400-77718400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr16:77717400-77719000 Enhancers Cortex derived primary cultured neurospheres brain
4 chr16:77717600-77718800 Enhancers Primary monocytes fromperipheralblood blood
5 chr16:77717600-77719000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr16:77717800-77718600 Flanking Active TSS Brain Germinal Matrix brain
7 chr16:77718000-77718400 Enhancers Brain Inferior Temporal Lobe brain
8 chr16:77718200-77718400 Flanking Active TSS Fetal Brain Female brain
9 chr16:77718200-77718600 Enhancers HUES64 Cell Line embryonic stem cell
10 chr16:77718200-77718600 Flanking Active TSS Fetal Lung lung
11 chr16:77718200-77718800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
12 chr16:77718200-77718800 Enhancers Pancreatic Islets Pancreatic Islet
13 chr16:77718200-77719000 Enhancers Monocytes-CD14+_RO01746 blood
14 chr16:77718200-77724200 Enhancers Fetal Brain Male brain

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