| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30065560-30066120 | Rare:176 | ||||
| chr16:30069660-30069917 | Common:1; Rare:90; Clinvar:1; Clinvar (benign):6 | ||||
| chr16:30075875-30076059 | Common:1; Rare:61 | ||||
| chr16:30122940-30123384 | Common:7; Rare:130 | ||||
| chr16:30183504-30183614 | Common:1; Rare:27 | ||||
| chr16:30355199-30355434 | Common:1; Rare:79 | ||||
| chr16:30355826-30355936 | Common:1; Rare:25 | ||||
| chr16:30407475-30407636 | Rare:55 | ||||
| chr16:30527281-30527702 | Common:1; Rare:106 | ||||
| chr16:30534834-30535095 | Common:3; Rare:84 | ||||
| chr16:30610373-30610529 | Rare:36 | ||||
| chr16:30698029-30698246 | Common:1; Rare:106 | ||||
| chr16:30698427-30698590 | Common:1; Rare:71 | ||||
| chr16:30748128-30748473 | Common:2; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30761433-30761564 | Rare:47 |