| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6828840-6829240 | Rare:128 | ||||
| chr12:6829556-6830001 | Common:4; Rare:172 | ||||
| chr12:6851247-6851497 | Rare:57 | ||||
| chr12:6851876-6852173 | Rare:77 | ||||
| chr12:6852314-6852689 | Common:1; Rare:94 | ||||
| chr12:6867336-6867532 | Common:2; Rare:72; Clinvar (benign):2 | ||||
| chr12:6873619-6874025 | Common:2; Rare:99 | ||||
| chr12:6904665-6905125 | Common:2; Rare:103 | ||||
| chr12:6914484-6914643 | Common:1; Rare:48 | ||||
| chr12:6915125-6915275 | Rare:34 | ||||
| chr12:6924887-6925179 | Common:11; Rare:70 | ||||
| chr12:6927420-6927850 | Rare:107 | ||||
| chr12:6937820-6938340 | Common:2; Rare:183; Clinvar (benign):1 | ||||
| chr12:6943517-6944089 | Common:17; Rare:427 | ||||
| chr12:6970617-6970996 | Common:4; Rare:123; Clinvar (benign):1 |