| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:17975602-17975765 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:18103372-18103485 | Rare:27 | ||||
| chr20:18299012-18299104 | Rare:15 | ||||
| chr20:18301031-18301207 | Rare:26 | ||||
| chr20:18520325-18520363 | Rare:5 | ||||
| chr20:18793974-18794097 | Rare:40 | ||||
| chr20:18921412-18921618 | Common:2; Rare:36 | ||||
| chr20:19758213-19758248 | Common:1; Rare:10 | ||||
| chr20:19884803-19884998 | Common:2; Rare:33 | ||||
| chr20:19988995-19989261 | Common:1; Rare:38 | ||||
| chr20:20026658-20026918 | Common:2; Rare:59 | ||||
| chr20:20032273-20032653 | Common:2; Rare:110 | ||||
| chr20:21205324-21205540 | Common:6; Rare:54 | ||||
| chr20:21330485-21330697 | Rare:58 | ||||
| chr20:21331566-21331815 | Common:2; Rare:59 |