| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6970312-6970450 | Common:1; Rare:51 | ||||
| chr12:6970566-6971053 | Common:9; Rare:156; Clinvar (benign):2 | ||||
| chr12:6971071-6971197 | Rare:39 | ||||
| chr12:6971340-6971412 | Rare:17 | ||||
| chr12:6981512-6981758 | Common:1; Rare:59 | ||||
| chr12:7018417-7018652 | Common:1; Rare:65 | ||||
| chr12:7018763-7019060 | Common:3; Rare:77 | ||||
| chr12:7060315-7060780 | Rare:95 | ||||
| chr12:7092376-7092665 | Rare:66 | ||||
| chr12:7108126-7108403 | Common:2; Rare:73 | ||||
| chr12:7108406-7108723 | Common:1; Rare:91 | ||||
| chr12:7108923-7109110 | Common:13; Rare:54 | ||||
| chr12:7109154-7109357 | Rare:64 | ||||
| chr12:7130264-7130415 | Common:4; Rare:40 | ||||
| chr12:7188995-7189220 | Common:2; Rare:49 |