Variant report

Variant rs772459
Chromosome Location chr12:56270199-56270200
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:56268000-56270200 Enhancers iPS-18 Cell Line embryonic stem cell
2 chr12:56268000-56270200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
3 chr12:56268200-56270200 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr12:56268400-56272200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr12:56268600-56271000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr12:56269200-56270200 Enhancers H1 Cell Line embryonic stem cell
7 chr12:56269400-56271400 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr12:56269600-56270200 Enhancers Cortex derived primary cultured neurospheres brain
9 chr12:56269800-56270200 Enhancers HUES6 Cell Line embryonic stem cell
10 chr12:56269800-56270200 Enhancers iPS-20b Cell Line embryonic stem cell
11 chr12:56269800-56270400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr12:56269800-56274600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
13 chr12:56270000-56270600 Enhancers HSMMtube muscle

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