| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:21501572-21501844 | Common:1; Rare:64 | ||||
| chr12:21657754-21658033 | Common:4; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:26938302-26938515 | Common:1; Rare:81 | ||||
| chr12:27524000-27524261 | Rare:64 | ||||
| chr12:38905588-38905726 | Common:3; Rare:38 | ||||
| chr12:42326065-42326220 | Common:1; Rare:49 | ||||
| chr12:43758753-43759013 | Common:2; Rare:74; Clinvar:2 | ||||
| chr12:45215994-45216154 | Rare:52 | ||||
| chr12:47705967-47706088 | Rare:56 | ||||
| chr12:48106034-48106104 | Rare:22 | ||||
| chr12:48716679-48717045 | Common:4; Rare:110 | ||||
| chr12:49018743-49018904 | Rare:62 | ||||
| chr12:49131334-49131606 | Common:2; Rare:108 | ||||
| chr12:49264752-49265133 | Common:5; Rare:137 | ||||
| chr12:49322937-49323323 | Common:3; Rare:100 |