| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110502051-110502331 | Common:1; Rare:101 | ||||
| chr12:110613953-110614335 | Rare:118; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:111685769-111686127 | Rare:133 | ||||
| chr12:111841875-111842038 | Common:2; Rare:47 | ||||
| chr12:112013093-112013474 | Common:1; Rare:134 | ||||
| chr12:112108725-112108845 | Rare:34 | ||||
| chr12:112906831-112907024 | Rare:39 | ||||
| chr12:113185426-113185748 | Common:8; Rare:125 | ||||
| chr12:113221019-113221319 | Common:2; Rare:86 | ||||
| chr12:113966306-113966527 | Common:8; Rare:76 | ||||
| chr12:114683714-114683905 | Common:1; Rare:32; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:114683906-114684269 | Common:4; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:114684518-114684671 | Rare:39 | ||||
| chr12:118135938-118136237 | Common:2; Rare:93 | ||||
| chr12:118372862-118373199 | Common:1; Rare:90 |