| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:44680250-44680640 | Common:1; Rare:95 | ||||
| chr18:44680691-44680894 | Common:1; Rare:59 | ||||
| chr18:44696977-44697213 | Common:1; Rare:58 | ||||
| chr18:45967237-45967513 | Rare:163; Clinvar (pathogenic):1 | ||||
| chr18:46098175-46098595 | Common:22; Rare:224; Clinvar (benign):13 | ||||
| chr18:46104225-46104412 | Common:6; Rare:92 | ||||
| chr18:46173919-46174152 | Common:2; Rare:107 | ||||
| chr18:46917424-46917609 | Rare:144 | ||||
| chr18:47150435-47150570 | Common:6; Rare:89 | ||||
| chr18:47176255-47176477 | Common:1; Rare:93; Clinvar (benign):2 | ||||
| chr18:47896290-47896626 | Rare:90 | ||||
| chr18:47930321-47930772 | Common:3; Rare:333 | ||||
| chr18:47930799-47931008 | Rare:117 | ||||
| chr18:47931016-47931320 | Rare:210 | ||||
| chr18:48538777-48539315 | Common:3; Rare:174 |