| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:14337561-14337685 | Rare:26 | ||||
| chr20:16573242-16573543 | Common:1; Rare:94 | ||||
| chr20:16729889-16730073 | Rare:55 | ||||
| chr20:17569135-17569197 | Rare:11 | ||||
| chr20:17569203-17569301 | Rare:18 | ||||
| chr20:17569949-17570210 | Common:3; Rare:115 | ||||
| chr20:17620181-17620367 | Rare:69 | ||||
| chr20:17682026-17682594 | Common:6; Rare:171 | ||||
| chr20:17968353-17968623 | Common:5; Rare:108 | ||||
| chr20:17968778-17969139 | Common:4; Rare:127 | ||||
| chr20:18466997-18467464 | Common:2; Rare:106 | ||||
| chr20:18507392-18507612 | Common:1; Rare:62; Clinvar:1 | ||||
| chr20:18507792-18507957 | Common:1; Rare:50; Clinvar:5; Clinvar (benign):1 | ||||
| chr20:19889291-19889612 | Common:3; Rare:71; Clinvar (benign):3 | ||||
| chr20:19934827-19935134 | Common:3; Rare:71; Clinvar (benign):3 |