| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:37178885-37179173 | Rare:83 | ||||
| chr20:37289578-37289669 | Common:1; Rare:28 | ||||
| chr20:37527821-37528168 | Common:3; Rare:121 | ||||
| chr20:38033397-38033775 | Common:2; Rare:111 | ||||
| chr20:38926187-38926417 | Common:1; Rare:78 | ||||
| chr20:38962106-38962382 | Common:2; Rare:114 | ||||
| chr20:41028562-41028886 | Rare:120 | ||||
| chr20:43457805-43457907 | Rare:45 | ||||
| chr20:43458250-43458420 | Common:2; Rare:67 | ||||
| chr20:43590625-43591004 | Rare:87 | ||||
| chr20:44210710-44211104 | Common:5; Rare:143 | ||||
| chr20:44475772-44475905 | Rare:56 | ||||
| chr20:44522015-44522222 | Common:2; Rare:66 | ||||
| chr20:44531792-44531977 | Common:1; Rare:59 | ||||
| chr20:44651662-44651854 | Common:1; Rare:50; Clinvar (benign):1 |