| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2004439-2004669 | Common:2; Rare:67 | ||||
| chr12:2794864-2795238 | Common:1; Rare:129 | ||||
| chr12:2796925-2797202 | Rare:68 | ||||
| chr12:2812891-2813029 | Rare:38 | ||||
| chr12:2877031-2877254 | Rare:68 | ||||
| chr12:3077266-3077438 | Common:6; Rare:76 | ||||
| chr12:4320969-4321253 | Common:5; Rare:105 | ||||
| chr12:4538452-4538813 | Rare:74 | ||||
| chr12:4649010-4649144 | Common:2; Rare:43; Clinvar (benign):1 | ||||
| chr12:6200042-6200559 | Common:4; Rare:152 | ||||
| chr12:6374821-6375536 | Common:6; Rare:187; Clinvar:2; Clinvar (benign):4 | ||||
| chr12:6376137-6376405 | Common:2; Rare:55 | ||||
| chr12:6383988-6384269 | Common:1; Rare:63 | ||||
| chr12:6452080-6452177 | Common:1; Rare:22 | ||||
| chr12:6493107-6493391 | Common:7; Rare:87 |