| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:71686260-71686640 | Common:4; Rare:165 | ||||
| chr12:71754691-71754944 | Common:5; Rare:123 | ||||
| chr12:71839633-71839806 | Common:2; Rare:127 | ||||
| chr12:74537722-74537985 | Common:2; Rare:145 | ||||
| chr12:75511569-75511877 | Rare:163 | ||||
| chr12:76031398-76031933 | Common:2; Rare:307 | ||||
| chr12:76083830-76084190 | Common:1; Rare:152 | ||||
| chr12:76084577-76084851 | Common:1; Rare:90 | ||||
| chr12:76348347-76348488 | Common:2; Rare:92; Clinvar:5; Clinvar (benign):2 | ||||
| chr12:76559494-76559949 | Common:2; Rare:252 | ||||
| chr12:76763936-76764285 | Common:7; Rare:285 | ||||
| chr12:77065301-77066054 | Common:5; Rare:317 | ||||
| chr12:79690247-79690713 | Common:4; Rare:227 | ||||
| chr12:79690896-79691253 | Common:2; Rare:247 | ||||
| chr12:79934180-79934610 | Common:2; Rare:143 |