| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:113184544-113184944 | Common:2; Rare:92 | ||||
| chr12:113184872-113185140 | Common:5; Rare:284 | ||||
| chr12:113185284-113185794 | Common:62; Rare:1041 | ||||
| chr12:113221021-113221560 | Common:21; Rare:807 | ||||
| chr12:113221731-113222131 | Common:3; Rare:105 | ||||
| chr12:113333905-113334761 | Common:7; Rare:211 | ||||
| chr12:113334987-113335718 | Rare:402 | ||||
| chr12:113357871-113358271 | Common:1; Rare:75 | ||||
| chr12:113358323-113358723 | Common:9; Rare:419 | ||||
| chr12:113358786-113359186 | Common:3; Rare:80 | ||||
| chr12:113403737-113404228 | Common:12; Rare:405 | ||||
| chr12:113421990-113422480 | Common:18; Rare:453 | ||||
| chr12:113966214-113966614 | Common:45; Rare:466 | ||||
| chr12:114684038-114684718 | Common:8; Rare:396; Clinvar:2 | ||||
| chr12:116276109-116277265 | Common:18; Rare:975; Clinvar (benign):8 |