| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:43590650-43590996 | Rare:78 | ||||
| chr20:44210386-44210464 | Rare:29 | ||||
| chr20:44210616-44211117 | Common:5; Rare:176 | ||||
| chr20:44475772-44475957 | Common:1; Rare:80 | ||||
| chr20:44521986-44522249 | Common:3; Rare:79 | ||||
| chr20:44531815-44531978 | Common:1; Rare:51 | ||||
| chr20:44582432-44582640 | Rare:33 | ||||
| chr20:44651662-44651839 | Common:1; Rare:49; Clinvar (benign):1 | ||||
| chr20:44885439-44885829 | Common:6; Rare:119 | ||||
| chr20:44960340-44960514 | Common:1; Rare:72 | ||||
| chr20:44966370-44966577 | Common:1; Rare:81 | ||||
| chr20:45348413-45348519 | Common:1; Rare:24 | ||||
| chr20:45362852-45363232 | Common:1; Rare:108 | ||||
| chr20:45363342-45363523 | Common:1; Rare:44 | ||||
| chr20:45406515-45406697 | Rare:52 |