| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:90102443-90102617 | Common:1; Rare:67 | ||||
| chr15:90233892-90234258 | Common:6; Rare:100 | ||||
| chr15:90717078-90717370 | Common:1; Rare:69 | ||||
| chr15:90884352-90884516 | Common:3; Rare:46 | ||||
| chr15:90994473-90994753 | Common:1; Rare:98 | ||||
| chr15:94231370-94231609 | Common:1; Rare:77 | ||||
| chr15:99251182-99251528 | Common:5; Rare:129 | ||||
| chr15:101295188-101295357 | Rare:52 | ||||
| chr16:53616-53897 | Common:7; Rare:82 | ||||
| chr16:78135-78249 | Common:2; Rare:41 | ||||
| chr16:397109-397302 | Common:4; Rare:54 | ||||
| chr16:760960-761134 | Common:2; Rare:56 | ||||
| chr16:1420728-1420997 | Common:1; Rare:108 | ||||
| chr16:2047815-2048033 | Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2268075-2268171 | Rare:42 |