| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110468693-110468915 | Rare:58 | ||||
| chr12:110502051-110502244 | Common:1; Rare:68 | ||||
| chr12:110613997-110614199 | Rare:61; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:110689381-110689494 | Rare:23 | ||||
| chr12:111685765-111686085 | Rare:121 | ||||
| chr12:111766805-111766973 | Rare:51 | ||||
| chr12:111841854-111842224 | Common:3; Rare:103 | ||||
| chr12:112013119-112013507 | Common:1; Rare:146 | ||||
| chr12:112791805-112791965 | Common:4; Rare:47 | ||||
| chr12:113185435-113185777 | Common:8; Rare:124 | ||||
| chr12:113966306-113966540 | Common:9; Rare:80 | ||||
| chr12:117190242-117190517 | Common:1; Rare:117 | ||||
| chr12:118016578-118016772 | Rare:38 | ||||
| chr12:118061066-118061135 | Rare:28 | ||||
| chr12:118135940-118136230 | Common:2; Rare:92 |