| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2835005-2835047 | Rare:14 | ||||
| chr12:2877031-2877253 | Rare:67 | ||||
| chr12:2890723-2890959 | Common:1; Rare:88 | ||||
| chr12:2959784-2959944 | Common:2; Rare:44 | ||||
| chr12:3873359-3873518 | Common:1; Rare:37 | ||||
| chr12:4320991-4321260 | Common:4; Rare:101 | ||||
| chr12:4538436-4538931 | Common:3; Rare:112 | ||||
| chr12:4648974-4649178 | Common:2; Rare:66; Clinvar (benign):2 | ||||
| chr12:6200139-6200446 | Common:4; Rare:97 | ||||
| chr12:6375239-6375668 | Common:5; Rare:108; Clinvar:1; Clinvar (benign):6 | ||||
| chr12:6452079-6452125 | Common:1; Rare:13 | ||||
| chr12:6493208-6493386 | Common:6; Rare:49 | ||||
| chr12:6493778-6494146 | Common:2; Rare:109 | ||||
| chr12:6534270-6534568 | Common:5; Rare:125 | ||||
| chr12:6568260-6568388 | Rare:50 |