| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118135924-118136245 | Common:2; Rare:97 | ||||
| chr12:118372846-118373165 | Common:2; Rare:83 | ||||
| chr12:119178610-119178829 | Rare:47 | ||||
| chr12:119668074-119668263 | Common:1; Rare:47 | ||||
| chr12:119711383-119711464 | Rare:11 | ||||
| chr12:119713550-119713973 | Common:2; Rare:98 | ||||
| chr12:120116607-120116970 | Common:6; Rare:110 | ||||
| chr12:120194687-120194798 | Rare:40 | ||||
| chr12:120201081-120201366 | Common:2; Rare:90 | ||||
| chr12:120225960-120226144 | Common:1; Rare:29 | ||||
| chr12:120250015-120250245 | Common:1; Rare:32 | ||||
| chr12:120327721-120328038 | Common:3; Rare:67 | ||||
| chr12:120438018-120438229 | Rare:93; Clinvar (benign):2 | ||||
| chr12:120446353-120446495 | Common:2; Rare:67 | ||||
| chr12:120469547-120469873 | Common:2; Rare:115 |