Variant report
| Variant | rs12606442 |
|---|---|
| Chromosome Location | chr18:30341925-30341926 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr18:30335600-30342200 | Enhancers | Primary B cells from peripheral blood | blood |
| 2 | chr18:30339400-30342200 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
| 3 | chr18:30339600-30342000 | Enhancers | H1 Cell Line | embryonic stem cell |
| 4 | chr18:30339600-30342000 | Enhancers | HUES48 Cell Line | embryonic stem cell |
| 5 | chr18:30339600-30342000 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
| 6 | chr18:30339600-30342200 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
| 7 | chr18:30340400-30343400 | Weak transcription | Fetal Brain Male | brain |
| 8 | chr18:30340800-30342000 | Enhancers | HUES64 Cell Line | embryonic stem cell |
| 9 | chr18:30341400-30345400 | Strong transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 10 | chr18:30341600-30342000 | Bivalent Enhancer | HUES6 Cell Line | embryonic stem cell |
| 11 | chr18:30341600-30342000 | Flanking Active TSS | Dnd41 | blood |
| 12 | chr18:30341600-30342600 | Enhancers | HepG2 | liver |
| 13 | chr18:30341800-30344200 | Weak transcription | Fetal Kidney | kidney |
| 14 | chr18:30341800-30347200 | Enhancers | Primary B cells from cord blood | blood |
