Variant report
| Variant | rs11977827 |
|---|---|
| Chromosome Location | chr7:99526316-99526317 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr7:99517600-99526800 | Weak transcription | Gastric | stomach |
| 2 | chr7:99517800-99526600 | Weak transcription | Esophagus | oesophagus |
| 3 | chr7:99517800-99526600 | Weak transcription | Fetal Muscle Trunk | muscle |
| 4 | chr7:99518000-99526600 | Weak transcription | Fetal Stomach | stomach |
| 5 | chr7:99518200-99526600 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
| 6 | chr7:99518200-99526800 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
| 7 | chr7:99518200-99526800 | Weak transcription | Brain Anterior Caudate | brain |
| 8 | chr7:99518200-99526800 | Weak transcription | Brain Hippocampus Middle | brain |
| 9 | chr7:99518200-99527000 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
| 10 | chr7:99518200-99527000 | Weak transcription | Brain Inferior Temporal Lobe | brain |
| 11 | chr7:99518400-99526800 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
| 12 | chr7:99518400-99526800 | Weak transcription | Rectal Smooth Muscle | rectum |
| 13 | chr7:99518600-99526400 | Weak transcription | Primary T helper naive cells from peripheral blood | blood |
| 14 | chr7:99519800-99526800 | Weak transcription | HSMM | muscle |
| 15 | chr7:99524400-99526600 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
| 16 | chr7:99524400-99526800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 17 | chr7:99524800-99526600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 18 | chr7:99525000-99526800 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 19 | chr7:99525000-99526800 | Weak transcription | HMEC | breast |
| 20 | chr7:99525600-99526600 | Bivalent Enhancer | Primary T regulatory cells fromperipheralblood | blood |
| 21 | chr7:99525600-99527000 | Enhancers | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 22 | chr7:99526200-99526400 | Bivalent Enhancer | K562 | blood |
| 23 | chr7:99526200-99526600 | Enhancers | Primary T helper naive cells fromperipheralblood | blood |
| 24 | chr7:99526200-99526800 | Enhancers | Primary T cells from cord blood | blood |
| 25 | chr7:99526200-99526800 | Bivalent Enhancer | Primary T cells fromperipheralblood | blood |
| 26 | chr7:99526200-99526800 | Enhancers | Primary T killer naive cells fromperipheralblood | blood |
| 27 | chr7:99526200-99526800 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 28 | chr7:99526200-99527000 | Flanking Active TSS | HepG2 | liver |
