| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118372914-118373192 | Common:1; Rare:63 | ||||
| chr12:120116720-120116935 | Common:2; Rare:71 | ||||
| chr12:120201081-120201354 | Common:2; Rare:88 | ||||
| chr12:120446344-120446470 | Common:1; Rare:56 | ||||
| chr12:120469587-120469867 | Common:2; Rare:102 | ||||
| chr12:120495900-120496216 | Common:6; Rare:104 | ||||
| chr12:120581353-120581559 | Common:1; Rare:76 | ||||
| chr12:122526922-122527282 | Common:3; Rare:111 | ||||
| chr12:122980571-122980950 | Common:2; Rare:108 | ||||
| chr12:123233127-123233490 | Common:2; Rare:114; Clinvar:1 | ||||
| chr12:123364831-123364969 | Common:2; Rare:55 | ||||
| chr12:123584336-123584687 | Common:7; Rare:127 | ||||
| chr12:123602023-123602156 | Common:3; Rare:47 | ||||
| chr12:123633624-123633845 | Common:1; Rare:101; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972573-123972894 | Common:6; Rare:113 |