| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:28176968-28177308 | Common:3; Rare:163 | ||||
| chr18:31101250-31101628 | Common:11; Rare:103 | ||||
| chr18:31101919-31102031 | Common:1; Rare:29; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr18:31102402-31102663 | Rare:63 | ||||
| chr18:31498050-31498337 | Common:1; Rare:102; Clinvar:8; Clinvar (benign):7 | ||||
| chr18:34493050-34493364 | Common:2; Rare:75 | ||||
| chr18:35290188-35290384 | Common:2; Rare:69 | ||||
| chr18:36129309-36129518 | Common:1; Rare:60 | ||||
| chr18:36129812-36129928 | Rare:46 | ||||
| chr18:36828740-36829141 | Common:3; Rare:154 | ||||
| chr18:45967261-45967465 | Rare:74 | ||||
| chr18:46098175-46098588 | Common:11; Rare:128; Clinvar (benign):8 | ||||
| chr18:46104135-46104399 | Common:3; Rare:75; Clinvar (benign):1 | ||||
| chr18:46756811-46757003 | Common:2; Rare:52 | ||||
| chr18:47150442-47150558 | Common:3; Rare:44 |