| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:2655530-2655726 | Common:4; Rare:98 | ||||
| chr18:2655834-2656217 | Common:4; Rare:126; Clinvar:6; Clinvar (benign):1 | ||||
| chr18:3013103-3013375 | Common:3; Rare:101 | ||||
| chr18:3247152-3247292 | Common:3; Rare:35 | ||||
| chr18:3247300-3247322 | Common:2; Rare:6 | ||||
| chr18:3247340-3247908 | Common:1; Rare:165 | ||||
| chr18:3261757-3262236 | Common:7; Rare:150 | ||||
| chr18:3447550-3447604 | Rare:11 | ||||
| chr18:3450059-3450243 | Common:1; Rare:53 | ||||
| chr18:3451517-3451675 | Common:2; Rare:59 | ||||
| chr18:4455156-4455562 | Common:3; Rare:148 | ||||
| chr18:5540393-5540536 | Rare:17 | ||||
| chr18:5543959-5544282 | Common:1; Rare:81 | ||||
| chr18:5630604-5630767 | Common:2; Rare:57 | ||||
| chr18:6326674-6326854 | Common:1; Rare:36 |