Variant report

Variant rs569694814
Chromosome Location chr12:38821290-38821291
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:38818800-38826200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr12:38819600-38821600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr12:38819800-38822200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
4 chr12:38820200-38821400 Enhancers HUES48 Cell Line embryonic stem cell
5 chr12:38820200-38821800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr12:38820200-38822400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr12:38820400-38821400 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr12:38820400-38822200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr12:38821200-38821600 Enhancers Cortex derived primary cultured neurospheres brain
10 chr12:38821200-38822000 Enhancers ES-I3 Cell Line embryonic stem cell

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