| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:54286705-54287101 | Common:3; Rare:113 | ||||
| chr16:56191092-56191376 | Common:4; Rare:101 | ||||
| chr16:56451259-56451614 | Common:1; Rare:116 | ||||
| chr16:56519769-56519871 | Rare:41; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr16:56519888-56520143 | Common:6; Rare:97; Clinvar:6; Clinvar (benign):7 | ||||
| chr16:56608315-56608428 | Common:1; Rare:25 | ||||
| chr16:56608429-56608760 | Common:3; Rare:99 | ||||
| chr16:56625616-56625875 | Rare:84 | ||||
| chr16:56625996-56626233 | Common:2; Rare:53 | ||||
| chr16:56638521-56638680 | Rare:64 | ||||
| chr16:56657573-56657821 | Rare:60 | ||||
| chr16:56657903-56658067 | Common:1; Rare:45 | ||||
| chr16:56682071-56682543 | Common:8; Rare:136 | ||||
| chr16:56729945-56730209 | Common:1; Rare:65 | ||||
| chr16:56931909-56932185 | Common:3; Rare:142 |