| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:14071017-14071344 | Common:3; Rare:108 | ||||
| chr16:14632687-14632989 | Common:1; Rare:105 | ||||
| chr16:15094229-15094478 | Common:1; Rare:126 | ||||
| chr16:15643026-15643267 | Rare:74 | ||||
| chr16:18801509-18801784 | Common:2; Rare:92 | ||||
| chr16:19067763-19067920 | Common:3; Rare:42 | ||||
| chr16:19113706-19113973 | Common:1; Rare:48 | ||||
| chr16:20325988-20326578 | Common:1; Rare:134 | ||||
| chr16:20326889-20327016 | Common:1; Rare:19 | ||||
| chr16:20327394-20328019 | Common:2; Rare:165 | ||||
| chr16:20676154-20676192 | Rare:6 | ||||
| chr16:20763937-20764072 | Common:2; Rare:23 | ||||
| chr16:20806331-20806536 | Rare:75 | ||||
| chr16:20900470-20900850 | Common:2; Rare:93 | ||||
| chr16:21952981-21953413 | Common:1; Rare:109; Clinvar (benign):3 |