| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:99251215-99251499 | Common:4; Rare:100 | ||||
| chr15:99565901-99566104 | Rare:94 | ||||
| chr15:100602162-100602534 | Common:3; Rare:97 | ||||
| chr15:101295135-101295350 | Rare:65 | ||||
| chr15:101652354-101652476 | Rare:55 | ||||
| chr16:53582-53911 | Common:7; Rare:112 | ||||
| chr16:970966-971192 | Common:6; Rare:96 | ||||
| chr16:1771502-1771862 | Common:3; Rare:141 | ||||
| chr16:1782508-1783012 | Common:4; Rare:166 | ||||
| chr16:1943189-1943491 | Common:1; Rare:91 | ||||
| chr16:1971904-1972113 | Common:1; Rare:61 | ||||
| chr16:2047795-2048038 | Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2155654-2155806 | Common:1; Rare:46 | ||||
| chr16:2268072-2268174 | Common:1; Rare:48 | ||||
| chr16:2474987-2475136 | Rare:49 |