| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51238648-51238914 | Common:8; Rare:115 | ||||
| chr12:51270188-51270257 | Common:1; Rare:19 | ||||
| chr12:51270282-51270312 | Rare:9 | ||||
| chr12:51391411-51391466 | Rare:10 | ||||
| chr12:51391613-51391803 | Common:3; Rare:58 | ||||
| chr12:52006797-52006942 | Rare:23 | ||||
| chr12:52051145-52051493 | Common:1; Rare:113 | ||||
| chr12:52191980-52192053 | Common:1; Rare:15 | ||||
| chr12:52233054-52233246 | Common:4; Rare:41 | ||||
| chr12:52233405-52233618 | Common:1; Rare:85 | ||||
| chr12:52452136-52452474 | Common:6; Rare:74 | ||||
| chr12:52520249-52520582 | Common:2; Rare:92; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr12:52905040-52905220 | Common:2; Rare:50 | ||||
| chr12:52949826-52949985 | Rare:36 | ||||
| chr12:53047023-53047347 | Common:1; Rare:81 |