| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31259755-31260155 | Rare:66 | ||||
| chr16:31354869-31355269 | Common:6; Rare:162 | ||||
| chr16:31371795-31372195 | Common:3; Rare:167 | ||||
| chr16:31427540-31427810 | Common:1; Rare:99 | ||||
| chr16:31442570-31443151 | Common:10; Rare:395 | ||||
| chr16:31443074-31443296 | Rare:52 | ||||
| chr16:31457842-31458498 | Common:6; Rare:445 | ||||
| chr16:31458980-31459230 | Common:1; Rare:234 | ||||
| chr16:31459220-31459590 | Common:7; Rare:671 | ||||
| chr16:31459630-31460135 | Common:2; Rare:629 | ||||
| chr16:31471728-31472283 | Rare:169 | ||||
| chr16:31484574-31484974 | Rare:165; Clinvar (pathogenic):3 | ||||
| chr16:31507763-31508171 | Common:3; Rare:331 | ||||
| chr16:31508250-31508717 | Common:25; Rare:610 | ||||
| chr16:31508843-31509243 | Common:1; Rare:77 |