| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:22297859-22298112 | Common:1; Rare:56 | ||||
| chr16:22374529-22374960 | Common:5; Rare:561 | ||||
| chr16:22436876-22437410 | Rare:783 | ||||
| chr16:22437448-22437820 | Common:11; Rare:196 | ||||
| chr16:23148552-23149044 | Common:6; Rare:340 | ||||
| chr16:23149207-23149698 | Common:11; Rare:492 | ||||
| chr16:23452480-23452814 | Rare:231; Clinvar (benign):1 | ||||
| chr16:23452781-23453295 | Rare:433; Clinvar:4; Clinvar (benign):6 | ||||
| chr16:23510323-23510998 | Common:17; Rare:442 | ||||
| chr16:23556919-23557770 | Common:21; Rare:1225; Clinvar:7; Clinvar (benign):20 | ||||
| chr16:23558086-23559210 | Common:9; Rare:380 | ||||
| chr16:23595509-23595909 | Common:3; Rare:96 | ||||
| chr16:23596154-23596554 | Common:5; Rare:379 | ||||
| chr16:23640631-23641031 | Common:1; Rare:79; Clinvar (benign):1 | ||||
| chr16:23641169-23641670 | Common:16; Rare:715; Clinvar:9; Clinvar (benign):33 |