| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122975153-122975241 | Common:1; Rare:22 | ||||
| chr12:122980571-122980743 | Common:1; Rare:56 | ||||
| chr12:123233093-123233490 | Common:2; Rare:132; Clinvar:1 | ||||
| chr12:123364800-123364977 | Common:3; Rare:71 | ||||
| chr12:123584317-123584622 | Common:6; Rare:107 | ||||
| chr12:123602031-123602151 | Common:3; Rare:41 | ||||
| chr12:123633624-123633860 | Common:1; Rare:110; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:124422655-124422792 | Common:2; Rare:36 | ||||
| chr12:131710855-131711113 | Rare:62 | ||||
| chr12:132687311-132687439 | Rare:55; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132887564-132887788 | Rare:67 | ||||
| chr12:132956260-132956383 | Common:1; Rare:28 | ||||
| chr12:133080739-133080943 | Rare:63 | ||||
| chr12:133130238-133130571 | Common:6; Rare:104 | ||||
| chr13:19181755-19182087 | Common:12; Rare:132 |