| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105107619-105107789 | Common:1; Rare:78 | ||||
| chr12:108561148-108561463 | Common:4; Rare:75 | ||||
| chr12:109477287-109477653 | Common:3; Rare:90 | ||||
| chr12:109573483-109573799 | Common:3; Rare:92; Clinvar:3; Clinvar (benign):5 | ||||
| chr12:110468715-110468909 | Rare:52 | ||||
| chr12:110502058-110502331 | Common:1; Rare:99 | ||||
| chr12:111685765-111686085 | Rare:121 | ||||
| chr12:111766853-111766971 | Rare:35 | ||||
| chr12:112013129-112013460 | Common:1; Rare:114 | ||||
| chr12:113185456-113185777 | Common:7; Rare:112 | ||||
| chr12:113966318-113966520 | Common:8; Rare:69 | ||||
| chr12:118016565-118016768 | Common:1; Rare:39 | ||||
| chr12:118135929-118136201 | Common:2; Rare:84 | ||||
| chr12:120116734-120116924 | Common:2; Rare:59 | ||||
| chr12:120201081-120201354 | Common:2; Rare:88 |