| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:18790234-18790461 | Common:4; Rare:83 | ||||
| chr16:19067415-19067646 | Common:4; Rare:75 | ||||
| chr16:19113750-19114048 | Common:1; Rare:64 | ||||
| chr16:20806349-20806614 | Rare:91 | ||||
| chr16:20900822-20900892 | Rare:16 | ||||
| chr16:21952997-21953409 | Common:1; Rare:106; Clinvar (benign):3 | ||||
| chr16:22008043-22008308 | Common:1; Rare:79 | ||||
| chr16:22374299-22374417 | Rare:40 | ||||
| chr16:22374546-22374876 | Common:1; Rare:123 | ||||
| chr16:22436949-22437055 | Rare:35 | ||||
| chr16:23557340-23557736 | Common:2; Rare:136; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641212-23641551 | Common:2; Rare:98; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:24818649-24818735 | Common:1; Rare:25 | ||||
| chr16:25111458-25111789 | Common:2; Rare:86 | ||||
| chr16:25257843-25257979 | Common:2; Rare:62 |