| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2284840-2285130 | Common:3; Rare:47 | ||||
| chr12:2397740-2398090 | Common:3; Rare:63 | ||||
| chr12:2613852-2613958 | Rare:14 | ||||
| chr12:2693132-2693565 | Common:2; Rare:103; Clinvar (benign):6 | ||||
| chr12:2784082-2784271 | Rare:53 | ||||
| chr12:2944570-2945020 | Common:4; Rare:80 | ||||
| chr12:2958593-2958743 | Common:2; Rare:39 | ||||
| chr12:3168660-3168970 | Common:4; Rare:65 | ||||
| chr12:3170711-3171111 | Common:2; Rare:109 | ||||
| chr12:3236973-3237081 | Rare:20 | ||||
| chr12:3304351-3304851 | Common:9; Rare:167 | ||||
| chr12:3310908-3311258 | Common:3; Rare:80 | ||||
| chr12:3336669-3336874 | Common:1; Rare:29 | ||||
| chr12:3337070-3337450 | Rare:63 | ||||
| chr12:3366108-3366252 | Rare:47 |