| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55929222-55929730 | Rare:195 | ||||
| chr12:55946582-55946982 | Common:1; Rare:94 | ||||
| chr12:55975204-55975466 | Common:1; Rare:42 | ||||
| chr12:55982637-55982795 | Common:1; Rare:16 | ||||
| chr12:56037265-56037665 | Rare:67 | ||||
| chr12:56118986-56119861 | Common:1; Rare:180 | ||||
| chr12:56126193-56126438 | Common:5; Rare:34 | ||||
| chr12:56129250-56129590 | Common:5; Rare:192 | ||||
| chr12:56187985-56188408 | Common:1; Rare:139 | ||||
| chr12:56190209-56190523 | Common:11; Rare:309 | ||||
| chr12:56336703-56336862 | Rare:36 | ||||
| chr12:56339502-56340109 | Common:2; Rare:285; Clinvar (benign):2 | ||||
| chr12:56341296-56341865 | Common:2; Rare:128 | ||||
| chr12:56358602-56359263 | Common:3; Rare:151 | ||||
| chr12:56360699-56361099 | Common:2; Rare:124 |