| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31073732-31073884 | Common:7; Rare:54 | ||||
| chr12:31729066-31729290 | Common:1; Rare:62 | ||||
| chr12:31959340-31959465 | Common:1; Rare:39 | ||||
| chr12:32679157-32679310 | Rare:56 | ||||
| chr12:42238178-42238472 | Common:1; Rare:98 | ||||
| chr12:42325988-42326212 | Common:1; Rare:72 | ||||
| chr12:43758745-43758991 | Common:2; Rare:67; Clinvar:2 | ||||
| chr12:43806253-43806425 | Common:2; Rare:61 | ||||
| chr12:45215987-45216163 | Common:1; Rare:58 | ||||
| chr12:46372715-46373004 | Rare:119 | ||||
| chr12:47079531-47079642 | Common:1; Rare:21 | ||||
| chr12:47705972-47706088 | Rare:55 | ||||
| chr12:48105791-48106222 | Common:3; Rare:130 | ||||
| chr12:48106231-48106373 | Rare:35 | ||||
| chr12:48119186-48119397 | Common:2; Rare:42; Clinvar:4; Clinvar (benign):2 |