| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31074187-31074438 | Common:1; Rare:68 | ||||
| chr16:31179820-31180199 | Common:3; Rare:163; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:31202686-31202935 | Common:2; Rare:92 | ||||
| chr16:31459310-31459517 | Common:1; Rare:85 | ||||
| chr16:31508369-31508490 | Common:4; Rare:49 | ||||
| chr16:46689130-46689416 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689506-46689724 | Common:2; Rare:92; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973561-46973789 | Rare:98 | ||||
| chr16:47461032-47461348 | Common:2; Rare:114; Clinvar (benign):2 | ||||
| chr16:48244253-48244322 | Common:1; Rare:16 | ||||
| chr16:53054808-53055068 | Common:2; Rare:59 | ||||
| chr16:53703815-53704206 | Common:1; Rare:121; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:56451274-56451610 | Common:1; Rare:107 | ||||
| chr16:56657925-56658061 | Common:1; Rare:35 | ||||
| chr16:56682376-56682560 | Common:4; Rare:73 |