| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:69585300-69585506 | Common:3; Rare:84 | ||||
| chr12:69738593-69738931 | Common:3; Rare:120 | ||||
| chr12:71663867-71664067 | Common:1; Rare:47 | ||||
| chr12:74537753-74537868 | Common:1; Rare:44 | ||||
| chr12:75390886-75391102 | Common:1; Rare:64 | ||||
| chr12:76083928-76084126 | Rare:59 | ||||
| chr12:76084568-76084794 | Common:1; Rare:75 | ||||
| chr12:76348359-76348521 | Common:1; Rare:60; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:76764013-76764261 | Common:2; Rare:101 | ||||
| chr12:76878937-76879312 | Rare:118 | ||||
| chr12:77065479-77065766 | Common:1; Rare:97 | ||||
| chr12:78864426-78864822 | Common:2; Rare:88 | ||||
| chr12:79045014-79045213 | Common:3; Rare:54 | ||||
| chr12:79690965-79691221 | Common:1; Rare:85 | ||||
| chr12:79934921-79935309 | Common:1; Rare:159 |