| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:23695020-23695268 | Rare:93 | ||||
| chr16:23706551-23706775 | Rare:37 | ||||
| chr16:23754596-23755113 | Common:2; Rare:114 | ||||
| chr16:24539429-24539627 | Common:1; Rare:78 | ||||
| chr16:24729478-24729844 | Common:7; Rare:139 | ||||
| chr16:25015291-25015461 | Common:2; Rare:62 | ||||
| chr16:25111521-25111852 | Common:2; Rare:104 | ||||
| chr16:25216726-25217238 | Common:3; Rare:132 | ||||
| chr16:25257290-25257608 | Common:1; Rare:99 | ||||
| chr16:27268713-27268850 | Common:1; Rare:46 | ||||
| chr16:27313206-27313513 | Common:1; Rare:48 | ||||
| chr16:27313804-27313993 | Common:2; Rare:52 | ||||
| chr16:27315363-27315531 | Common:1; Rare:36 | ||||
| chr16:27549706-27550177 | Common:2; Rare:173 | ||||
| chr16:28491907-28492132 | Common:2; Rare:52; Clinvar:2; Clinvar (benign):2 |