| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:3752414-3752704 | Common:2; Rare:62 | ||||
| chr12:3752908-3753288 | Common:4; Rare:94 | ||||
| chr12:3873067-3873239 | Rare:51 | ||||
| chr12:3873396-3873581 | Common:2; Rare:46 | ||||
| chr12:4307930-4308131 | Common:2; Rare:51 | ||||
| chr12:4320861-4321272 | Common:5; Rare:156 | ||||
| chr12:4538275-4538937 | Common:3; Rare:155 | ||||
| chr12:4604600-4604950 | Common:6; Rare:82 | ||||
| chr12:4648286-4648509 | Common:1; Rare:45 | ||||
| chr12:4648826-4649174 | Common:2; Rare:93; Clinvar (benign):2 | ||||
| chr12:6199982-6200386 | Common:3; Rare:113 | ||||
| chr12:6201284-6201482 | Common:2; Rare:47 | ||||
| chr12:6310492-6310737 | Common:4; Rare:66 | ||||
| chr12:6312723-6312930 | Common:2; Rare:48 | ||||
| chr12:6341982-6342114 | Rare:27; Clinvar (benign):1 |