| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:48930240-48930450 | Common:1; Rare:45 | ||||
| chr18:48942664-48942929 | Common:2; Rare:99 | ||||
| chr18:48948679-48948900 | Rare:115 | ||||
| chr18:49460530-49460812 | Common:4; Rare:158; Clinvar:12; Clinvar (benign):2 | ||||
| chr18:49487167-49487423 | Common:6; Rare:193 | ||||
| chr18:49491610-49492160 | Common:4; Rare:222 | ||||
| chr18:49813480-49813610 | Rare:32 | ||||
| chr18:49813514-49813654 | Rare:30 | ||||
| chr18:49813814-49814314 | Common:3; Rare:360 | ||||
| chr18:50281421-50281579 | Rare:113 | ||||
| chr18:50287608-50287733 | Common:1; Rare:48 | ||||
| chr18:50374876-50375171 | Common:7; Rare:176 | ||||
| chr18:50878935-50879254 | Common:8; Rare:202 | ||||
| chr18:50967885-50968089 | Rare:125 | ||||
| chr18:51030036-51030288 | Rare:164; Clinvar:6 |