| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:96489397-96489642 | Common:3; Rare:64 | ||||
| chr12:96907140-96907290 | Common:1; Rare:52 | ||||
| chr12:98515536-98516141 | Common:2; Rare:227; Clinvar:12; Clinvar (benign):10 | ||||
| chr12:98644703-98644843 | Common:3; Rare:47 | ||||
| chr12:98645013-98645307 | Common:2; Rare:88 | ||||
| chr12:100267054-100267291 | Common:1; Rare:111 | ||||
| chr12:100573554-100573785 | Rare:79 | ||||
| chr12:101407663-101408049 | Common:3; Rare:95 | ||||
| chr12:101877515-101877795 | Common:5; Rare:73 | ||||
| chr12:102120060-102120269 | Common:1; Rare:85 | ||||
| chr12:103930057-103930571 | Common:8; Rare:172 | ||||
| chr12:103965698-103965941 | Common:2; Rare:58 | ||||
| chr12:104064457-104064555 | Rare:27 | ||||
| chr12:104138164-104138418 | Common:1; Rare:75 | ||||
| chr12:104286770-104287192 | Common:4; Rare:74 |