| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109477293-109477437 | Common:3; Rare:49 | ||||
| chr12:109573470-109573863 | Common:3; Rare:117; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr12:110614004-110614166 | Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:111685996-111686138 | Rare:45 | ||||
| chr12:111841915-111842254 | Common:2; Rare:93 | ||||
| chr12:112013129-112013492 | Common:1; Rare:133 | ||||
| chr12:113185439-113185773 | Common:8; Rare:118 | ||||
| chr12:118061095-118061283 | Common:1; Rare:47 | ||||
| chr12:118135946-118136302 | Common:2; Rare:109 | ||||
| chr12:118372785-118373171 | Common:2; Rare:102 | ||||
| chr12:120116746-120116924 | Common:2; Rare:55 | ||||
| chr12:120201078-120201357 | Common:2; Rare:89 | ||||
| chr12:120437896-120438127 | Common:2; Rare:70; Clinvar (benign):1 | ||||
| chr12:120446268-120446477 | Common:1; Rare:78 | ||||
| chr12:120469689-120469868 | Common:1; Rare:60 |