| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118103815-118104092 | Common:1; Rare:66 | ||||
| chr12:118135941-118136268 | Common:2; Rare:97 | ||||
| chr12:118372865-118373216 | Common:1; Rare:96 | ||||
| chr12:118376530-118376793 | Rare:83 | ||||
| chr12:119877269-119877512 | Common:2; Rare:55 | ||||
| chr12:120116627-120116974 | Common:6; Rare:111 | ||||
| chr12:120194683-120194781 | Rare:34 | ||||
| chr12:120201081-120201366 | Common:2; Rare:90 | ||||
| chr12:120437850-120438229 | Common:2; Rare:142; Clinvar (benign):2 | ||||
| chr12:120446289-120446495 | Common:2; Rare:84 | ||||
| chr12:120469437-120469873 | Common:5; Rare:142 | ||||
| chr12:120495867-120496236 | Common:7; Rare:124 | ||||
| chr12:120529129-120529390 | Common:1; Rare:61 | ||||
| chr12:120581358-120581427 | Rare:39 | ||||
| chr12:120686967-120687157 | Common:1; Rare:65 |