| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6318197-6318384 | Rare:56 | ||||
| chr12:6318519-6318759 | Common:2; Rare:59 | ||||
| chr12:6330860-6331018 | Rare:41; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6341603-6341655 | Rare:6 | ||||
| chr12:6356372-6356529 | Common:1; Rare:26 | ||||
| chr12:6375042-6375672 | Common:7; Rare:156; Clinvar:1; Clinvar (benign):6 | ||||
| chr12:6383974-6384309 | Common:2; Rare:81 | ||||
| chr12:6386134-6386440 | Rare:76 | ||||
| chr12:6452016-6452287 | Common:1; Rare:61 | ||||
| chr12:6452914-6453120 | Common:2; Rare:48 | ||||
| chr12:6470641-6470785 | Common:1; Rare:48 | ||||
| chr12:6493088-6493386 | Common:7; Rare:88 | ||||
| chr12:6493539-6493630 | Common:2; Rare:13 | ||||
| chr12:6493772-6494151 | Common:2; Rare:112 | ||||
| chr12:6534270-6534569 | Common:5; Rare:126 |