| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6200005-6200559 | Common:4; Rare:166 | ||||
| chr12:6310526-6310737 | Common:4; Rare:54 | ||||
| chr12:6317340-6317656 | Common:1; Rare:114 | ||||
| chr12:6330909-6331108 | Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6341703-6341758 | Common:1; Rare:19 | ||||
| chr12:6348955-6349123 | Common:1; Rare:44; Clinvar (pathogenic):1 | ||||
| chr12:6356222-6356533 | Common:1; Rare:46 | ||||
| chr12:6376119-6376414 | Common:2; Rare:61 | ||||
| chr12:6383968-6384282 | Common:2; Rare:76 | ||||
| chr12:6386153-6386380 | Rare:52 | ||||
| chr12:6444809-6445020 | Common:1; Rare:34 | ||||
| chr12:6451785-6452077 | Common:3; Rare:50 | ||||
| chr12:6452079-6452212 | Common:1; Rare:32 | ||||
| chr12:6452933-6453118 | Common:1; Rare:43 | ||||
| chr12:6470633-6470937 | Common:2; Rare:89 |