| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:10435274-10435485 | Rare:65 | ||||
| chr20:10673933-10674532 | Common:5; Rare:184; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:11890630-11890926 | Common:2; Rare:109 | ||||
| chr20:11890938-11891091 | Common:1; Rare:51 | ||||
| chr20:11891261-11891473 | Rare:65 | ||||
| chr20:11917628-11917926 | Common:1; Rare:49 | ||||
| chr20:13638692-13639119 | Common:3; Rare:129 | ||||
| chr20:13784831-13785134 | Common:3; Rare:136; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:13785231-13785408 | Common:4; Rare:83; Clinvar:2; Clinvar (benign):6 | ||||
| chr20:15985278-15985456 | Common:4; Rare:33 | ||||
| chr20:15985920-15986155 | Rare:49 | ||||
| chr20:16573273-16573579 | Common:1; Rare:91 | ||||
| chr20:16729812-16730129 | Common:3; Rare:98 | ||||
| chr20:17569747-17570158 | Common:5; Rare:134 | ||||
| chr20:17681503-17681720 | Common:2; Rare:53 |