| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2835013-2835081 | Rare:23 | ||||
| chr12:2877027-2877262 | Rare:70 | ||||
| chr12:2890697-2890972 | Common:1; Rare:110 | ||||
| chr12:2959843-2959944 | Common:1; Rare:26 | ||||
| chr12:3077206-3077445 | Common:7; Rare:97 | ||||
| chr12:3753053-3753249 | Common:1; Rare:49 | ||||
| chr12:3873307-3873493 | Common:4; Rare:36 | ||||
| chr12:4273918-4274235 | Common:1; Rare:85; Clinvar (benign):1 | ||||
| chr12:4275433-4275578 | Common:2; Rare:20 | ||||
| chr12:4276203-4276261 | Rare:18 | ||||
| chr12:4320942-4321266 | Common:5; Rare:125 | ||||
| chr12:4538440-4538934 | Common:3; Rare:111 | ||||
| chr12:4649010-4649178 | Common:2; Rare:57; Clinvar (benign):2 | ||||
| chr12:5043767-5044038 | Common:3; Rare:70; Clinvar (benign):1 | ||||
| chr12:6124515-6124762 | Rare:35; Clinvar:2 |