Variant report
| Variant | rs34247947 |
|---|---|
| Chromosome Location | chr11:71054701-71054702 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr11:71053000-71054800 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 2 | chr11:71053000-71054800 | Enhancers | HMEC | breast |
| 3 | chr11:71053000-71056600 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 4 | chr11:71053200-71054800 | Enhancers | IMR90 fetal lung fibroblasts Cell Line | lung |
| 5 | chr11:71054000-71055000 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
| 6 | chr11:71054200-71054800 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 7 | chr11:71054200-71054800 | Enhancers | Placenta Amnion | Placenta Amnion |
| 8 | chr11:71054400-71054800 | Enhancers | Pancreas | Pancrea |
| 9 | chr11:71054400-71054800 | Enhancers | A549 | lung |
| 10 | chr11:71054400-71054800 | Flanking Bivalent TSS/Enh | HepG2 | liver |
| 11 | chr11:71054400-71055000 | Enhancers | Fetal Intestine Large | intestine |
| 12 | chr11:71054400-71055000 | Enhancers | Fetal Intestine Small | intestine |
| 13 | chr11:71054400-71055200 | Enhancers | Brain Inferior Temporal Lobe | brain |
| 14 | chr11:71054400-71055600 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
| 15 | chr11:71054600-71054800 | Enhancers | Brain Germinal Matrix | brain |
| 16 | chr11:71054600-71055000 | Enhancers | Primary B cells from peripheral blood | blood |
| 17 | chr11:71054600-71055000 | Bivalent Enhancer | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 18 | chr11:71054600-71055000 | Enhancers | Liver | Liver |
| 19 | chr11:71054600-71055000 | Enhancers | Rectal Mucosa Donor 29 | rectum |
| 20 | chr11:71054600-71055000 | Enhancers | Spleen | Spleen |
| 21 | chr11:71054600-71055200 | Enhancers | Brain Cingulate Gyrus | brain |
| 22 | chr11:71054600-71055400 | Enhancers | iPS DF 6.9 Cell Line | embryonic stem cell |
