No. |
Chromosome Location |
Chromatin state |
Cell line |
Tissue |
1 |
chr13:50411400-50422000 |
Weak transcription |
iPS DF 6.9 Cell Line |
embryonic stem cell
|
2 |
chr13:50413000-50421600 |
Weak transcription |
Foreskin Keratinocyte Primary Cells skin03 |
Skin
|
3 |
chr13:50413400-50418600 |
Weak transcription |
Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells |
embryonic stem cell
|
4 |
chr13:50415000-50418200 |
Weak transcription |
Foreskin Fibroblast Primary Cells skin02 |
Skin
|
5 |
chr13:50415000-50418400 |
Weak transcription |
Primary hematopoietic stem cells short term culture |
blood
|
6 |
chr13:50415000-50420600 |
Weak transcription |
K562 |
blood
|
7 |
chr13:50415400-50421600 |
Weak transcription |
HepG2 |
liver
|
8 |
chr13:50415400-50421800 |
Weak transcription |
Fetal Adrenal Gland |
Adrenal Gland
|
9 |
chr13:50415600-50421800 |
Weak transcription |
H9 Cell Line |
embryonic stem cell
|
10 |
chr13:50416200-50416400 |
Enhancers |
Osteobl |
bone
|
11 |
chr13:50416200-50416600 |
Enhancers |
Foreskin Fibroblast Primary Cells skin01 |
Skin
|