Variant report
| Variant | rs1415817 |
|---|---|
| Chromosome Location | chr20:22492606-22492607 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr20:22490000-22496000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr20:22491800-22494400 | Enhancers | Fetal Intestine Large | intestine |
| 3 | chr20:22492000-22492800 | Enhancers | Liver | Liver |
| 4 | chr20:22492000-22493400 | Enhancers | Rectal Mucosa Donor 31 | rectum |
| 5 | chr20:22492200-22494200 | Flanking Active TSS | HepG2 | liver |
| 6 | chr20:22492200-22494400 | Enhancers | Fetal Intestine Small | intestine |
| 7 | chr20:22492400-22493200 | Enhancers | Pancreatic Islets | Pancreatic Islet |
| 8 | chr20:22492400-22493800 | Enhancers | Fetal Lung | lung |
| 9 | chr20:22492400-22493800 | Enhancers | K562 | blood |
| 10 | chr20:22492400-22494000 | Enhancers | HUVEC | blood vessel |
| 11 | chr20:22492400-22494600 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
| 12 | chr20:22492400-22494600 | Enhancers | Stomach Mucosa | stomach |
| 13 | chr20:22492600-22492800 | Bivalent Enhancer | iPS-18 Cell Line | embryonic stem cell |
| 14 | chr20:22492600-22492800 | Bivalent Enhancer | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 15 | chr20:22492600-22492800 | Bivalent Enhancer | Placenta Amnion | Placenta Amnion |
| 16 | chr20:22492600-22493000 | Enhancers | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
| 17 | chr20:22492600-22493400 | Enhancers | Placenta | Placenta |
| 18 | chr20:22492600-22493600 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
| 19 | chr20:22492600-22493600 | Enhancers | Sigmoid Colon | Sigmoid Colon |
| 20 | chr20:22492600-22493800 | Flanking Active TSS | A549 | lung |
| 21 | chr20:22492600-22494200 | Enhancers | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 22 | chr20:22492600-22494600 | Enhancers | Pancreas | Pancrea |
