| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120201081-120201366 | Common:2; Rare:90 | ||||
| chr12:120437927-120438222 | Common:2; Rare:115; Clinvar (benign):2 | ||||
| chr12:120446344-120446478 | Common:1; Rare:60 | ||||
| chr12:120469518-120469895 | Common:4; Rare:128 | ||||
| chr12:120495845-120496249 | Common:7; Rare:134 | ||||
| chr12:120529094-120529233 | Common:2; Rare:53 | ||||
| chr12:120581358-120581586 | Common:1; Rare:79 | ||||
| chr12:121209931-121210161 | Common:5; Rare:76 | ||||
| chr12:121399907-121400180 | Common:3; Rare:105 | ||||
| chr12:121802908-121803091 | Rare:48 | ||||
| chr12:121888632-121888874 | Common:2; Rare:78 | ||||
| chr12:122225739-122225773 | Rare:7 | ||||
| chr12:122526856-122527291 | Common:4; Rare:160 | ||||
| chr12:122896058-122896231 | Rare:89 | ||||
| chr12:122975207-122975252 | Rare:16 |