| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:1811730-1811876 | Common:1; Rare:33 | ||||
| chr12:2795023-2795203 | Rare:74 | ||||
| chr12:2798966-2799237 | Common:1; Rare:67 | ||||
| chr12:2800865-2801274 | Common:2; Rare:102 | ||||
| chr12:2812607-2812755 | Common:1; Rare:55 | ||||
| chr12:2812880-2812927 | Rare:23 | ||||
| chr12:2812929-2813062 | Rare:28 | ||||
| chr12:2877031-2877253 | Rare:67 | ||||
| chr12:2959843-2959964 | Common:1; Rare:31 | ||||
| chr12:3077206-3077443 | Common:7; Rare:96 | ||||
| chr12:3873355-3873535 | Common:1; Rare:40 | ||||
| chr12:4273918-4274229 | Common:1; Rare:84; Clinvar (benign):1 | ||||
| chr12:4275455-4275566 | Common:2; Rare:14 | ||||
| chr12:4320949-4321258 | Common:5; Rare:117 | ||||
| chr12:4538440-4538934 | Common:3; Rare:111 |