| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:27313804-27314012 | Common:2; Rare:57 | ||||
| chr16:27315268-27315531 | Common:1; Rare:51 | ||||
| chr16:27402057-27402342 | Common:2; Rare:70 | ||||
| chr16:27402488-27402582 | Common:1; Rare:19 | ||||
| chr16:27549886-27550167 | Common:2; Rare:104 | ||||
| chr16:28491432-28491516 | Rare:34; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:28491912-28492116 | Common:2; Rare:49; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:28494230-28494288 | Rare:8 | ||||
| chr16:28494539-28494738 | Rare:52 | ||||
| chr16:28506829-28507089 | Rare:55 | ||||
| chr16:28538815-28538833 | Rare:3 | ||||
| chr16:28538878-28539317 | Common:2; Rare:91 | ||||
| chr16:28553869-28554011 | Common:3; Rare:49 | ||||
| chr16:28554138-28554369 | Common:4; Rare:89 | ||||
| chr16:28597038-28597246 | Common:1; Rare:58 |