| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44187017-44187354 | Common:4; Rare:76 | ||||
| chr20:44187475-44187745 | Common:1; Rare:47 | ||||
| chr20:44210590-44211111 | Common:5; Rare:181 | ||||
| chr20:44475791-44475945 | Rare:66 | ||||
| chr20:44521980-44522355 | Common:3; Rare:96 | ||||
| chr20:44582052-44582373 | Common:1; Rare:60 | ||||
| chr20:44651687-44651798 | Common:1; Rare:32; Clinvar (benign):1 | ||||
| chr20:44885602-44885876 | Common:4; Rare:90 | ||||
| chr20:44966341-44966571 | Common:2; Rare:91 | ||||
| chr20:45362948-45363276 | Rare:101 | ||||
| chr20:45363357-45363548 | Common:2; Rare:52 | ||||
| chr20:45405754-45406098 | Common:2; Rare:78 | ||||
| chr20:45406537-45406892 | Rare:90 | ||||
| chr20:45407007-45407025 | Rare:2 | ||||
| chr20:45407274-45407341 | Rare:17 |