Variant report
| Variant | rs183024529 |
|---|---|
| Chromosome Location | chr14:69483721-69483722 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr14:69473000-69503600 | Weak transcription | Right Atrium | heart |
| 2 | chr14:69481000-69486000 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 3 | chr14:69481200-69484800 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
| 4 | chr14:69481400-69484200 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
| 5 | chr14:69481800-69484800 | Weak transcription | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
| 6 | chr14:69481800-69484800 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
| 7 | chr14:69481800-69484800 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
| 8 | chr14:69481800-69485000 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
| 9 | chr14:69482000-69484200 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
| 10 | chr14:69482000-69484600 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
| 11 | chr14:69482000-69484800 | Weak transcription | HepG2 | liver |
| 12 | chr14:69482000-69485200 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 13 | chr14:69482400-69485200 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
| 14 | chr14:69483200-69485600 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
| 15 | chr14:69483400-69484000 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
| 16 | chr14:69483600-69483800 | Enhancers | iPS DF 6.9 Cell Line | embryonic stem cell |
| 17 | chr14:69483600-69484800 | Weak transcription | K562 | blood |
