| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:84689676-84689967 | Common:2; Rare:60 | ||||
| chr12:97464953-97465249 | Rare:50 | ||||
| chr12:107903688-107903883 | Common:5; Rare:66 | ||||
| chr12:110282621-110282790 | Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:110936446-110936598 | Rare:44 | ||||
| chr12:120291901-120292189 | Common:8; Rare:113 | ||||
| chr12:121578527-121578750 | Common:1; Rare:34 | ||||
| chr12:121582265-121582362 | Rare:12 | ||||
| chr12:123270277-123270564 | Common:3; Rare:84 | ||||
| chr12:124141841-124142093 | Rare:45 | ||||
| chr12:130875715-130875923 | Common:2; Rare:45 | ||||
| chr13:32745683-32745998 | Common:1; Rare:67 | ||||
| chr13:35857848-35858065 | Common:3; Rare:41 | ||||
| chr13:42870834-42870883 | Rare:12 | ||||
| chr13:42872287-42872646 | Rare:95 |