Variant report
Variant | rs522066 |
---|---|
Chromosome Location | chr6:143055157-143055158 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:143049400-143056600 | Weak transcription | Esophagus | oesophagus |
2 | chr6:143049800-143073200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr6:143050000-143058200 | Weak transcription | NHEK | skin |
4 | chr6:143050000-143061600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
5 | chr6:143050400-143058000 | Weak transcription | Pancreas | Pancrea |
6 | chr6:143050600-143058600 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
7 | chr6:143050800-143058600 | Weak transcription | NHDF-Ad | bronchial |
8 | chr6:143051200-143056600 | Weak transcription | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
9 | chr6:143053000-143056600 | Weak transcription | Placenta | Placenta |
10 | chr6:143054200-143072800 | Weak transcription | Primary T cells from cord blood | blood |
11 | chr6:143055000-143056200 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |