Variant report
| Variant | rs2141765 |
|---|---|
| Chromosome Location | chr12:64919976-64919977 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:64912400-64927600 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
| 2 | chr12:64915000-64922400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 3 | chr12:64916600-64925400 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
| 4 | chr12:64916800-64922400 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 5 | chr12:64916800-64925400 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
| 6 | chr12:64916800-64925400 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
| 7 | chr12:64916800-64925600 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
| 8 | chr12:64917000-64925600 | Weak transcription | H1 Cell Line | embryonic stem cell |
| 9 | chr12:64917400-64920600 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
| 10 | chr12:64917400-64920600 | Weak transcription | NHDF-Ad | bronchial |
| 11 | chr12:64917400-64922400 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 12 | chr12:64917800-64921800 | Weak transcription | Dnd41 | blood |
| 13 | chr12:64919400-64920200 | Enhancers | Fetal Brain Male | brain |
| 14 | chr12:64919800-64926600 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
