| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2340243-2340365 | Rare:47 | ||||
| chr16:2340615-2341118 | Common:10; Rare:424; Clinvar:9; Clinvar (benign):6 | ||||
| chr16:2428941-2429521 | Common:11; Rare:443 | ||||
| chr16:2459879-2460240 | Common:6; Rare:289 | ||||
| chr16:2474878-2475184 | Common:1; Rare:243; Clinvar (benign):10 | ||||
| chr16:2513524-2514164 | Common:1; Rare:562 | ||||
| chr16:2519070-2519648 | Common:2; Rare:254 | ||||
| chr16:2520199-2520530 | Common:19; Rare:415 | ||||
| chr16:2531837-2532372 | Common:12; Rare:333 | ||||
| chr16:2537585-2538126 | Common:13; Rare:527 | ||||
| chr16:2682269-2682697 | Rare:491 | ||||
| chr16:2719934-2720432 | Common:2; Rare:234 | ||||
| chr16:2720989-2721630 | Common:4; Rare:344 | ||||
| chr16:2752100-2752493 | Common:3; Rare:246 | ||||
| chr16:2752433-2753190 | Common:10; Rare:719 |