| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30527258-30527569 | Common:1; Rare:88 | ||||
| chr16:30534873-30535107 | Common:3; Rare:78 | ||||
| chr16:30571558-30571718 | Rare:47 | ||||
| chr16:30572131-30572268 | Rare:46 | ||||
| chr16:30585525-30585942 | Common:1; Rare:94 | ||||
| chr16:30610341-30610652 | Rare:76 | ||||
| chr16:30623715-30623758 | Rare:11 | ||||
| chr16:30623800-30623825 | Rare:3 | ||||
| chr16:30623934-30624281 | Common:1; Rare:60 | ||||
| chr16:30650555-30650796 | Rare:46 | ||||
| chr16:30698100-30698239 | Rare:83 | ||||
| chr16:30698449-30698647 | Common:1; Rare:78 | ||||
| chr16:30699046-30699392 | Rare:84; Clinvar (benign):1 | ||||
| chr16:30748128-30748441 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30762052-30762346 | Common:3; Rare:94 |