| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:19067415-19067715 | Common:5; Rare:124; Clinvar:1 | ||||
| chr16:19067755-19068017 | Common:3; Rare:72 | ||||
| chr16:19521972-19522214 | Rare:61 | ||||
| chr16:19523818-19523977 | Common:2; Rare:24 | ||||
| chr16:19555494-19555732 | Common:2; Rare:110 | ||||
| chr16:20741755-20741996 | Common:1; Rare:104 | ||||
| chr16:20806317-20806694 | Rare:113 | ||||
| chr16:20900226-20900716 | Common:3; Rare:109 | ||||
| chr16:20900756-20901060 | Common:3; Rare:78 | ||||
| chr16:21158510-21158712 | Common:1; Rare:59 | ||||
| chr16:21952991-21953419 | Common:1; Rare:109; Clinvar (benign):3 | ||||
| chr16:22436923-22437113 | Rare:70 | ||||
| chr16:22437517-22437580 | Rare:21 | ||||
| chr16:23452699-23452831 | Rare:49; Clinvar (benign):1 | ||||
| chr16:23453126-23453250 | Rare:35 |