Variant report
Variant | rs3943980 |
---|---|
Chromosome Location | chr4:106676766-106676767 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:106634000-106693200 | Weak transcription | K562 | blood |
2 | chr4:106659400-106679400 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
3 | chr4:106659400-106686400 | Weak transcription | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
4 | chr4:106659600-106691800 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
5 | chr4:106661400-106686600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
6 | chr4:106661400-106686600 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
7 | chr4:106661600-106696800 | Weak transcription | Fetal Intestine Small | intestine |
8 | chr4:106663800-106688600 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
9 | chr4:106668600-106679800 | Weak transcription | Brain Hippocampus Middle | brain |
10 | chr4:106673200-106686600 | Weak transcription | GM12878-XiMat | blood |
11 | chr4:106673600-106678600 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |