| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:68808402-68809287 | Common:18; Rare:739; Clinvar:5 | ||||
| chr12:69239324-69239724 | Common:13; Rare:616 | ||||
| chr12:69348170-69348453 | Common:4; Rare:102; Clinvar (benign):3 | ||||
| chr12:69359206-69360336 | Common:58; Rare:1147 | ||||
| chr12:69470142-69470542 | Common:18; Rare:453 | ||||
| chr12:69470677-69471077 | Common:5; Rare:102 | ||||
| chr12:69585191-69585591 | Common:23; Rare:648 | ||||
| chr12:69585746-69586004 | Common:2; Rare:124 | ||||
| chr12:69689000-69689500 | Common:10; Rare:159 | ||||
| chr12:69738568-69738968 | Common:9; Rare:332 | ||||
| chr12:69739353-69739712 | Common:7; Rare:72 | ||||
| chr12:70242530-70243180 | Common:18; Rare:749 | ||||
| chr12:70243120-70244490 | Common:31; Rare:1136 | ||||
| chr12:70366004-70366404 | Common:4; Rare:191 | ||||
| chr12:70366590-70367080 | Common:1; Rare:109 |