| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:43513965-43514156 | Rare:80 | ||||
| chr20:43514205-43514590 | Common:1; Rare:121 | ||||
| chr20:43514797-43514945 | Common:3; Rare:45 | ||||
| chr20:43590826-43591003 | Rare:47 | ||||
| chr20:43666929-43667170 | Common:2; Rare:92 | ||||
| chr20:43914699-43914892 | Common:3; Rare:55 | ||||
| chr20:43915968-43916081 | Rare:20 | ||||
| chr20:44210581-44211140 | Common:5; Rare:192 | ||||
| chr20:44311067-44311312 | Common:1; Rare:97 | ||||
| chr20:44475739-44475988 | Common:1; Rare:102 | ||||
| chr20:44521957-44522270 | Common:3; Rare:92 | ||||
| chr20:44531756-44531926 | Common:1; Rare:57 | ||||
| chr20:44582425-44582650 | Rare:35 | ||||
| chr20:44651075-44651210 | Common:1; Rare:23 | ||||
| chr20:44651646-44652048 | Common:1; Rare:106; Clinvar (benign):1 |