| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31135764-31135843 | Rare:17 | ||||
| chr16:31142188-31142682 | Common:2; Rare:132 | ||||
| chr16:31179677-31180266 | Common:4; Rare:252; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:31180544-31180862 | Common:3; Rare:119 | ||||
| chr16:31355035-31355215 | Common:1; Rare:46 | ||||
| chr16:31442831-31442916 | Rare:15 | ||||
| chr16:31442960-31443205 | Common:1; Rare:54 | ||||
| chr16:31458177-31458602 | Common:2; Rare:135 | ||||
| chr16:31458650-31458726 | Common:1; Rare:20 | ||||
| chr16:31458772-31458990 | Common:1; Rare:61 | ||||
| chr16:31459024-31459218 | Rare:49 | ||||
| chr16:31459237-31459588 | Common:2; Rare:140 | ||||
| chr16:31459630-31460103 | Common:1; Rare:227 | ||||
| chr16:31471788-31471986 | Rare:36 | ||||
| chr16:31472040-31472251 | Rare:59 |