| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98593469-98593771 | Common:2; Rare:99; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98645007-98645293 | Common:2; Rare:87 | ||||
| chr12:102120071-102120210 | Rare:52 | ||||
| chr12:103965698-103965941 | Common:2; Rare:58 | ||||
| chr12:104064435-104064543 | Rare:23 | ||||
| chr12:104138182-104138415 | Common:1; Rare:68 | ||||
| chr12:104287218-104287350 | Rare:34 | ||||
| chr12:105107615-105107785 | Common:1; Rare:77 | ||||
| chr12:107685717-107685828 | Rare:37 | ||||
| chr12:108339304-108339432 | Common:1; Rare:36 | ||||
| chr12:109477332-109477653 | Common:3; Rare:64 | ||||
| chr12:109573483-109573832 | Common:3; Rare:98; Clinvar:3; Clinvar (benign):5 | ||||
| chr12:110502067-110502198 | Common:1; Rare:47 | ||||
| chr12:112013129-112013460 | Common:1; Rare:114 | ||||
| chr12:113185456-113185769 | Common:7; Rare:110 |