| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:103802329-103802682 | Common:4; Rare:46 | ||||
| chr12:103841060-103841497 | Common:6; Rare:142 | ||||
| chr12:103930022-103930571 | Common:9; Rare:181 | ||||
| chr12:103930577-103930882 | Common:5; Rare:68 | ||||
| chr12:103957103-103957349 | Common:7; Rare:66 | ||||
| chr12:103965690-103966009 | Common:3; Rare:78 | ||||
| chr12:104064435-104064555 | Rare:29 | ||||
| chr12:104138134-104138421 | Common:1; Rare:79 | ||||
| chr12:104286793-104287451 | Common:4; Rare:143 | ||||
| chr12:104288718-104289044 | Common:1; Rare:123 | ||||
| chr12:104958254-104958391 | Common:3; Rare:39 | ||||
| chr12:104986199-104986376 | Common:4; Rare:65 | ||||
| chr12:105107612-105107824 | Common:1; Rare:98; Clinvar:1 | ||||
| chr12:105236063-105236352 | Common:3; Rare:134 | ||||
| chr12:106357387-106357827 | Common:4; Rare:75; Clinvar:2; Clinvar (benign):1 |