| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:22374564-22374911 | Common:1; Rare:120 | ||||
| chr16:22436908-22437069 | Rare:56 | ||||
| chr16:22437120-22437410 | Rare:91 | ||||
| chr16:23149400-23149770 | Common:2; Rare:117 | ||||
| chr16:23452530-23452940 | Rare:119; Clinvar:2; Clinvar (benign):3 | ||||
| chr16:23453162-23453284 | Rare:34 | ||||
| chr16:23557313-23557633 | Common:3; Rare:113; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23596278-23596476 | Common:1; Rare:51 | ||||
| chr16:23641257-23641543 | Common:2; Rare:83; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23678671-23678953 | Common:5; Rare:86 | ||||
| chr16:23694990-23695250 | Rare:102 | ||||
| chr16:24539418-24539590 | Rare:67 | ||||
| chr16:24729601-24729732 | Common:6; Rare:70 | ||||
| chr16:24730093-24730414 | Common:1; Rare:108 | ||||
| chr16:25014582-25014824 | Rare:47 |