| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109477293-109477653 | Common:3; Rare:85 | ||||
| chr12:109573478-109573813 | Common:3; Rare:99; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:109900209-109900356 | Rare:59 | ||||
| chr12:109996285-109996439 | Common:2; Rare:43 | ||||
| chr12:110468691-110468909 | Rare:56 | ||||
| chr12:110502055-110502218 | Common:1; Rare:58 | ||||
| chr12:112013125-112013466 | Common:1; Rare:121 | ||||
| chr12:113185415-113185768 | Common:9; Rare:135 | ||||
| chr12:113966306-113966506 | Common:7; Rare:67 | ||||
| chr12:116910844-116911008 | Rare:60 | ||||
| chr12:118135995-118136184 | Common:2; Rare:50 | ||||
| chr12:120116725-120116907 | Rare:56 | ||||
| chr12:120194683-120194804 | Rare:45 | ||||
| chr12:120201085-120201326 | Common:2; Rare:79 | ||||
| chr12:120446353-120446470 | Common:1; Rare:53 |