| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:58629772-58630032 | Common:1; Rare:74 | ||||
| chr16:58734234-58734408 | Common:4; Rare:54 | ||||
| chr16:66552468-66552635 | Rare:74 | ||||
| chr16:66880348-66880580 | Common:1; Rare:65 | ||||
| chr16:66934347-66934499 | Common:1; Rare:58 | ||||
| chr16:67028899-67029118 | Rare:91 | ||||
| chr16:67109802-67109997 | Rare:62 | ||||
| chr16:67159873-67159977 | Rare:17 | ||||
| chr16:67183945-67184036 | Common:1; Rare:29 | ||||
| chr16:67192079-67192221 | Rare:49 | ||||
| chr16:67227008-67227167 | Rare:63 | ||||
| chr16:67481136-67481448 | Common:2; Rare:99 | ||||
| chr16:67561986-67562306 | Rare:103 | ||||
| chr16:67644820-67645223 | Common:2; Rare:90 | ||||
| chr16:67660222-67660391 | Rare:105; Clinvar:2; Clinvar (benign):2 |