| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:29381132-29381304 | Common:2; Rare:58 | ||||
| chr12:30754762-30755041 | Common:1; Rare:112 | ||||
| chr12:31073732-31073896 | Common:7; Rare:61 | ||||
| chr12:31074088-31074285 | Common:1; Rare:39 | ||||
| chr12:31326090-31326439 | Common:4; Rare:120 | ||||
| chr12:31729010-31729267 | Rare:74 | ||||
| chr12:31959132-31959490 | Common:3; Rare:102 | ||||
| chr12:31959502-31959838 | Common:3; Rare:120 | ||||
| chr12:32399750-32399912 | Common:1; Rare:59 | ||||
| chr12:32896753-32896979 | Common:1; Rare:76; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:38905506-38905742 | Common:3; Rare:62 | ||||
| chr12:38906269-38906350 | Common:1; Rare:19 | ||||
| chr12:38906713-38906832 | Common:1; Rare:25 | ||||
| chr12:39443101-39443220 | Common:1; Rare:29; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:42238153-42238490 | Common:2; Rare:110 |