| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108515039-108515313 | Common:1; Rare:82 | ||||
| chr12:108538140-108538354 | Common:3; Rare:52 | ||||
| chr12:108857571-108857850 | Common:3; Rare:130 | ||||
| chr12:109093428-109093512 | Rare:34 | ||||
| chr12:109130988-109131180 | Common:1; Rare:34 | ||||
| chr12:109477261-109477664 | Common:3; Rare:107 | ||||
| chr12:109573436-109573790 | Common:3; Rare:118; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880361-109880668 | Common:1; Rare:92 | ||||
| chr12:109900195-109900348 | Rare:63 | ||||
| chr12:109996299-109996450 | Common:2; Rare:42 | ||||
| chr12:110280482-110280732 | Rare:60 | ||||
| chr12:110281024-110281193 | Rare:66 | ||||
| chr12:110450254-110450443 | Common:2; Rare:71 | ||||
| chr12:110502051-110502241 | Common:1; Rare:66 | ||||
| chr12:111685724-111686119 | Rare:140 |