| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30123154-30123362 | Common:5; Rare:56 | ||||
| chr16:30355210-30355354 | Common:1; Rare:56 | ||||
| chr16:30445871-30446056 | Common:1; Rare:45 | ||||
| chr16:30527258-30527482 | Rare:65 | ||||
| chr16:30534535-30534633 | Common:1; Rare:40 | ||||
| chr16:30534675-30535089 | Common:3; Rare:128 | ||||
| chr16:30571535-30571652 | Rare:43 | ||||
| chr16:30585510-30585902 | Common:1; Rare:91 | ||||
| chr16:30658646-30658866 | Common:1; Rare:66 | ||||
| chr16:30697859-30698246 | Common:1; Rare:160 | ||||
| chr16:30698455-30698653 | Common:1; Rare:77 | ||||
| chr16:30699035-30699372 | Rare:83; Clinvar (benign):1 | ||||
| chr16:30748128-30748447 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30762060-30762357 | Common:3; Rare:97 | ||||
| chr16:30787144-30787219 | Rare:14 |