| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98644726-98644843 | Common:2; Rare:38 | ||||
| chr12:98644944-98645293 | Common:2; Rare:103 | ||||
| chr12:100200489-100200834 | Common:6; Rare:97 | ||||
| chr12:100267045-100267293 | Common:1; Rare:117 | ||||
| chr12:100573601-100573740 | Rare:42 | ||||
| chr12:101407690-101408085 | Common:3; Rare:94 | ||||
| chr12:102120048-102120283 | Common:1; Rare:95 | ||||
| chr12:103930033-103930557 | Common:9; Rare:176 | ||||
| chr12:103965664-103965941 | Common:2; Rare:73 | ||||
| chr12:104064339-104064543 | Common:1; Rare:46 | ||||
| chr12:104138142-104138379 | Common:1; Rare:58 | ||||
| chr12:104288720-104288932 | Common:1; Rare:87 | ||||
| chr12:104986208-104986370 | Common:3; Rare:59 | ||||
| chr12:105107612-105107803 | Common:1; Rare:91; Clinvar:1 | ||||
| chr12:106357645-106357814 | Common:3; Rare:38; Clinvar:2; Clinvar (benign):1 |