| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2004408-2004510 | Rare:44 | ||||
| chr12:2053454-2053598 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:2812374-2812713 | Common:1; Rare:75 | ||||
| chr12:2812885-2813017 | Rare:39 | ||||
| chr12:2835013-2835043 | Rare:11 | ||||
| chr12:2876949-2877253 | Rare:91 | ||||
| chr12:2959194-2959431 | Rare:64 | ||||
| chr12:2959802-2959944 | Common:1; Rare:39 | ||||
| chr12:3077246-3077439 | Common:7; Rare:83 | ||||
| chr12:3873307-3873514 | Common:4; Rare:44 | ||||
| chr12:4320943-4321266 | Common:5; Rare:125 | ||||
| chr12:4538436-4538798 | Rare:75 | ||||
| chr12:4648992-4649178 | Common:2; Rare:61; Clinvar (benign):2 | ||||
| chr12:6199565-6199882 | Common:1; Rare:61 | ||||
| chr12:6199996-6200559 | Common:4; Rare:169 |