Variant report
Variant | rs9693399 |
---|---|
Chromosome Location | chr8:130366696-130366697 |
allele | A/C |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:130355000-130368400 | Strong transcription | K562 | blood |
2 | chr8:130361600-130368400 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
3 | chr8:130361600-130370800 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
4 | chr8:130361800-130371000 | Weak transcription | Primary monocytes fromperipheralblood | blood |
5 | chr8:130365200-130374800 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
6 | chr8:130365800-130368400 | Weak transcription | Fetal Thymus | thymus |
7 | chr8:130365800-130377400 | Weak transcription | Dnd41 | blood |