| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:45967261-45967465 | Rare:74 | ||||
| chr18:46104135-46104406 | Common:4; Rare:79; Clinvar (benign):1 | ||||
| chr18:46174203-46174228 | Rare:6 | ||||
| chr18:48538940-48539192 | Common:1; Rare:64 | ||||
| chr18:49487147-49487303 | Common:3; Rare:56 | ||||
| chr18:49490452-49490935 | Common:1; Rare:119 | ||||
| chr18:49813493-49813617 | Rare:28 | ||||
| chr18:49813821-49814308 | Common:2; Rare:195 | ||||
| chr18:50273403-50273638 | Common:1; Rare:67; Clinvar (benign):1 | ||||
| chr18:50275960-50276295 | Common:2; Rare:80 | ||||
| chr18:50281453-50281899 | Common:3; Rare:150 | ||||
| chr18:50878936-50879220 | Common:4; Rare:94 | ||||
| chr18:50967884-50968064 | Rare:64 | ||||
| chr18:51030054-51030244 | Rare:63 | ||||
| chr18:54269273-54269617 | Common:3; Rare:127 |