| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32731295-32732318 | Common:8; Rare:319; Clinvar:4; Clinvar (benign):6 | ||||
| chr12:32740184-32740606 | Common:4; Rare:222; Clinvar:2; Clinvar (benign):5 | ||||
| chr12:32755110-32755410 | Common:3; Rare:215; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr12:32755795-32756083 | Common:2; Rare:222 | ||||
| chr12:32896671-32897023 | Common:7; Rare:254; Clinvar:14; Clinvar (benign):14 | ||||
| chr12:32896970-32897347 | Common:2; Rare:101 | ||||
| chr12:33439071-33439242 | Rare:47 | ||||
| chr12:33439473-33440538 | Common:14; Rare:467 | ||||
| chr12:34022127-34022653 | Common:5; Rare:181 | ||||
| chr12:39442220-39442760 | Common:1; Rare:101 | ||||
| chr12:39443042-39443477 | Common:5; Rare:260; Clinvar:18; Clinvar (benign):13 | ||||
| chr12:40105946-40106401 | Common:3; Rare:250 | ||||
| chr12:40224792-40224975 | Common:4; Rare:47 | ||||
| chr12:40225130-40225490 | Common:1; Rare:92; Clinvar (benign):1 | ||||
| chr12:42144591-42145104 | Common:28; Rare:541 |