| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106955635-106956054 | Common:3; Rare:144 | ||||
| chr12:107685695-107685882 | Rare:67 | ||||
| chr12:108561153-108561411 | Common:2; Rare:61 | ||||
| chr12:109477298-109477410 | Common:2; Rare:39 | ||||
| chr12:109573483-109573860 | Common:3; Rare:108; Clinvar:5; Clinvar (benign):6 | ||||
| chr12:110450271-110450490 | Common:2; Rare:71 | ||||
| chr12:110502069-110502236 | Common:1; Rare:58 | ||||
| chr12:111685788-111686104 | Rare:122 | ||||
| chr12:111841908-111842257 | Common:2; Rare:97 | ||||
| chr12:112013128-112013477 | Common:1; Rare:123 | ||||
| chr12:113185440-113185769 | Common:8; Rare:117 | ||||
| chr12:116738017-116738327 | Common:5; Rare:102 | ||||
| chr12:118061109-118061281 | Common:1; Rare:38 | ||||
| chr12:118135990-118136266 | Common:2; Rare:73 | ||||
| chr12:118372813-118373197 | Common:2; Rare:104 |