| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123364820-123364977 | Common:3; Rare:61 | ||||
| chr12:123584317-123584813 | Common:9; Rare:166 | ||||
| chr12:123602031-123602156 | Common:3; Rare:44 | ||||
| chr12:123633607-123633851 | Common:1; Rare:117; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:124422649-124422829 | Common:2; Rare:48 | ||||
| chr12:124914819-124915096 | Common:3; Rare:110 | ||||
| chr12:130871714-130872126 | Common:4; Rare:172 | ||||
| chr12:131710782-131711107 | Rare:88 | ||||
| chr12:132687387-132687689 | Common:4; Rare:104 | ||||
| chr12:132829052-132829247 | Rare:88 | ||||
| chr12:132887553-132887788 | Rare:74 | ||||
| chr12:132956252-132956410 | Common:1; Rare:36 | ||||
| chr12:132986236-132986428 | Rare:40 | ||||
| chr12:133037220-133037536 | Common:4; Rare:64 | ||||
| chr12:133080143-133080453 | Common:7; Rare:98 |