| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:389242-389347 | Rare:40 | ||||
| chr12:389453-389667 | Common:5; Rare:83 | ||||
| chr12:401440-401664 | Rare:61 | ||||
| chr12:2004435-2004669 | Common:2; Rare:69 | ||||
| chr12:2812609-2812714 | Common:1; Rare:35 | ||||
| chr12:2812884-2812941 | Rare:24 | ||||
| chr12:2877022-2877254 | Rare:69 | ||||
| chr12:3077243-3077445 | Common:7; Rare:85 | ||||
| chr12:4273908-4274233 | Common:1; Rare:88; Clinvar (benign):1 | ||||
| chr12:4275748-4276077 | Rare:68 | ||||
| chr12:4320949-4321296 | Common:5; Rare:135 | ||||
| chr12:4538440-4538907 | Common:1; Rare:102 | ||||
| chr12:4648994-4649154 | Common:2; Rare:54; Clinvar (benign):1 | ||||
| chr12:6124407-6124764 | Rare:53; Clinvar:2 | ||||
| chr12:6200005-6200559 | Common:4; Rare:166 |