| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105184645-105184687 | Rare:7 | ||||
| chr12:106247367-106247428 | Rare:14 | ||||
| chr12:106962695-106962808 | Common:1; Rare:20 | ||||
| chr12:107708976-107709224 | Common:2; Rare:70 | ||||
| chr12:108530275-108530543 | Rare:66; Clinvar:1 | ||||
| chr12:108536719-108536961 | Rare:59 | ||||
| chr12:108852684-108852896 | Rare:52 | ||||
| chr12:109053946-109054143 | Rare:37 | ||||
| chr12:109110949-109111535 | Common:2; Rare:147; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:110025444-110025583 | Rare:10 | ||||
| chr12:111663016-111663102 | Rare:9 | ||||
| chr12:111770381-111770454 | Rare:15 | ||||
| chr12:111780759-111780826 | Common:1; Rare:10 | ||||
| chr12:111867505-111867650 | Rare:39 | ||||
| chr12:111870194-111870346 | Rare:41 |