| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:11890670-11890897 | Common:2; Rare:86 | ||||
| chr20:13638881-13639117 | Common:2; Rare:83 | ||||
| chr20:13784845-13785112 | Common:3; Rare:124; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:13785277-13785437 | Common:3; Rare:78; Clinvar (benign):5 | ||||
| chr20:13990605-13990683 | Rare:15 | ||||
| chr20:13995148-13995610 | Common:1; Rare:129 | ||||
| chr20:14337515-14337588 | Rare:19 | ||||
| chr20:14337591-14337680 | Rare:17 | ||||
| chr20:14523254-14523407 | Rare:24 | ||||
| chr20:16573283-16573558 | Common:1; Rare:80 | ||||
| chr20:16729915-16730073 | Rare:46 | ||||
| chr20:17569218-17569272 | Rare:11 | ||||
| chr20:17569966-17570210 | Common:3; Rare:108 | ||||
| chr20:17643036-17643406 | Common:2; Rare:92 | ||||
| chr20:17682112-17682574 | Common:6; Rare:147 |