| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105107612-105107802 | Common:1; Rare:90; Clinvar:1 | ||||
| chr12:105236075-105236277 | Common:2; Rare:92 | ||||
| chr12:109477287-109477656 | Common:3; Rare:91 | ||||
| chr12:109573433-109573821 | Common:3; Rare:126; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880371-109880668 | Common:1; Rare:91 | ||||
| chr12:110468715-110468909 | Rare:52 | ||||
| chr12:110502058-110502247 | Common:1; Rare:67 | ||||
| chr12:110613997-110614195 | Rare:58; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:111685736-111686127 | Rare:142 | ||||
| chr12:111766814-111766972 | Rare:48 | ||||
| chr12:111841887-111842241 | Common:3; Rare:97 | ||||
| chr12:112013137-112013468 | Common:1; Rare:116 | ||||
| chr12:112108769-112108807 | Rare:10 | ||||
| chr12:113185426-113185576 | Common:7; Rare:65 | ||||
| chr12:118135990-118136175 | Common:2; Rare:51 |