| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43826918-43827044 | Rare:57 | ||||
| chr15:44288386-44288737 | Common:38; Rare:215 | ||||
| chr15:44427559-44427653 | Rare:28 | ||||
| chr15:44536663-44536740 | Rare:15 | ||||
| chr15:44536855-44537209 | Common:1; Rare:125 | ||||
| chr15:44663543-44663689 | Rare:84; Clinvar:12; Clinvar (benign):6 | ||||
| chr15:44711347-44711611 | Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44728869-44729193 | Common:1; Rare:68 | ||||
| chr15:45023052-45023243 | Common:3; Rare:52 | ||||
| chr15:45114147-45114326 | Common:2; Rare:36 | ||||
| chr15:45200489-45200656 | Common:1; Rare:47 | ||||
| chr15:45201066-45201153 | Common:2; Rare:35 | ||||
| chr15:45378481-45378658 | Common:4; Rare:51; Clinvar:1; Clinvar (benign):4 | ||||
| chr15:45587084-45587474 | Common:1; Rare:95; Clinvar:6; Clinvar (benign):1 | ||||
| chr15:47184053-47184282 | Common:1; Rare:68 |