| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31509254-31510039 | Common:6; Rare:308 | ||||
| chr16:31527606-31528006 | Common:5; Rare:128 | ||||
| chr16:31712850-31713387 | Common:4; Rare:217 | ||||
| chr16:31873501-31873954 | Common:3; Rare:380 | ||||
| chr16:31874186-31874754 | Common:1; Rare:124 | ||||
| chr16:46620633-46621068 | Common:4; Rare:168 | ||||
| chr16:46621237-46621637 | Common:3; Rare:341 | ||||
| chr16:46688594-46688789 | Rare:87 | ||||
| chr16:46689025-46689448 | Common:7; Rare:728; Clinvar:14; Clinvar (benign):7 | ||||
| chr16:46689460-46689730 | Common:14; Rare:627; Clinvar:1; Clinvar (benign):14; Clinvar (pathogenic):5 | ||||
| chr16:46689997-46690397 | Common:1; Rare:128 | ||||
| chr16:46690885-46691285 | Rare:107; Clinvar:2 | ||||
| chr16:46748223-46748623 | Rare:135 | ||||
| chr16:46748706-46749141 | Common:2; Rare:152 | ||||
| chr16:46789774-46790201 | Common:26; Rare:350 |