| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7189474-7189780 | Common:3; Rare:245; Clinvar:12; Clinvar (benign):1 | ||||
| chr12:7891087-7891370 | Common:1; Rare:90 | ||||
| chr12:8032452-8033193 | Common:14; Rare:374 | ||||
| chr12:8033312-8033740 | Rare:253 | ||||
| chr12:8697502-8698298 | Common:11; Rare:559 | ||||
| chr12:8913940-8914500 | Common:9; Rare:262 | ||||
| chr12:8914770-8915160 | Common:1; Rare:93 | ||||
| chr12:8949377-8949862 | Common:3; Rare:206 | ||||
| chr12:8949862-8950130 | Common:7; Rare:156 | ||||
| chr12:10111380-10111780 | Common:10; Rare:151 | ||||
| chr12:10130050-10130630 | Common:4; Rare:106 | ||||
| chr12:10170065-10170606 | Common:6; Rare:187 | ||||
| chr12:10212240-10212910 | Common:10; Rare:308 | ||||
| chr12:10613488-10613737 | Common:3; Rare:266 | ||||
| chr12:10673983-10674460 | Common:3; Rare:136 |