| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:79934551-79934651 | Rare:25 | ||||
| chr12:79935034-79935396 | Common:1; Rare:130 | ||||
| chr12:79935679-79935805 | Rare:28 | ||||
| chr12:80936687-80936907 | Common:1; Rare:53 | ||||
| chr12:80937685-80937807 | Common:1; Rare:37 | ||||
| chr12:82358341-82358600 | Rare:129 | ||||
| chr12:82358702-82358909 | Common:3; Rare:108 | ||||
| chr12:82686378-82686579 | Rare:47 | ||||
| chr12:82686618-82687193 | Common:3; Rare:159 | ||||
| chr12:82687321-82687370 | Rare:12 | ||||
| chr12:82687712-82687916 | Common:1; Rare:49 | ||||
| chr12:88035215-88035640 | Common:4; Rare:94 | ||||
| chr12:88035760-88035825 | Rare:20 | ||||
| chr12:88141761-88141830 | Common:1; Rare:12 | ||||
| chr12:88141836-88141934 | Common:1; Rare:16; Clinvar:2; Clinvar (benign):1 |