| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:17470438-17470550 | Common:2; Rare:30; Clinvar (benign):1 | ||||
| chr16:18784810-18784860 | Rare:14 | ||||
| chr16:18801432-18801582 | Common:1; Rare:69; Clinvar:1 | ||||
| chr16:18801584-18801816 | Common:2; Rare:64 | ||||
| chr16:19067414-19067667 | Common:5; Rare:92 | ||||
| chr16:19067808-19067929 | Common:2; Rare:31 | ||||
| chr16:19113634-19113945 | Common:1; Rare:51 | ||||
| chr16:20763925-20764010 | Common:2; Rare:14 | ||||
| chr16:20806426-20806651 | Rare:73 | ||||
| chr16:20900300-20900786 | Common:3; Rare:106 | ||||
| chr16:20900800-20900914 | Common:1; Rare:35 | ||||
| chr16:21158562-21158740 | Common:1; Rare:54 | ||||
| chr16:21303030-21303235 | Rare:40 | ||||
| chr16:21599362-21599814 | Common:4; Rare:165 | ||||
| chr16:21952975-21953445 | Common:1; Rare:117; Clinvar (benign):3 |