| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:12702627-12703083 | Common:3; Rare:177 | ||||
| chr18:12884143-12884425 | Common:4; Rare:145 | ||||
| chr18:12947660-12948061 | Common:3; Rare:104 | ||||
| chr18:12991134-12991417 | Common:2; Rare:104 | ||||
| chr18:13218674-13218786 | Common:1; Rare:24 | ||||
| chr18:13726462-13726718 | Common:3; Rare:101 | ||||
| chr18:21111028-21111090 | Rare:14 | ||||
| chr18:21600632-21600828 | Rare:48 | ||||
| chr18:22169305-22169630 | Common:2; Rare:88 | ||||
| chr18:22169860-22170023 | Rare:27 | ||||
| chr18:22170781-22170902 | Common:1; Rare:17 | ||||
| chr18:22933150-22933395 | Common:3; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:22933800-22933867 | Common:1; Rare:26 | ||||
| chr18:23453187-23453352 | Rare:56 | ||||
| chr18:23503298-23503621 | Common:4; Rare:136 |