| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:29381136-29381352 | Common:2; Rare:69 | ||||
| chr12:30695860-30695977 | Common:1; Rare:30 | ||||
| chr12:30754762-30755082 | Common:1; Rare:131 | ||||
| chr12:31073776-31073892 | Rare:47 | ||||
| chr12:31324098-31324240 | Rare:36 | ||||
| chr12:31326111-31326460 | Common:4; Rare:120 | ||||
| chr12:31729012-31729267 | Rare:74 | ||||
| chr12:31959282-31959490 | Common:2; Rare:65 | ||||
| chr12:32679050-32679344 | Common:2; Rare:112; Clinvar (benign):3 | ||||
| chr12:32755875-32756015 | Rare:48 | ||||
| chr12:38905560-38905798 | Common:5; Rare:64 | ||||
| chr12:38906712-38906847 | Common:1; Rare:31 | ||||
| chr12:42238164-42238481 | Common:1; Rare:104 | ||||
| chr12:42325964-42326207 | Common:1; Rare:76 | ||||
| chr12:43758745-43759000 | Common:2; Rare:70; Clinvar:2 |