| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:76053085-76053352 | Common:1; Rare:68 | ||||
| chr12:76084565-76084801 | Common:1; Rare:78 | ||||
| chr12:76348334-76348565 | Common:2; Rare:86; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559487-76559978 | Common:2; Rare:159 | ||||
| chr12:76763892-76764294 | Common:5; Rare:168 | ||||
| chr12:76878929-76879198 | Rare:94 | ||||
| chr12:77065463-77065914 | Common:3; Rare:148 | ||||
| chr12:78864572-78864822 | Common:2; Rare:55 | ||||
| chr12:79690360-79690679 | Common:1; Rare:88 | ||||
| chr12:79690896-79691052 | Rare:50 | ||||
| chr12:79691056-79691176 | Rare:37 | ||||
| chr12:79820832-79821163 | Rare:84 | ||||
| chr12:79934370-79934667 | Common:1; Rare:65 | ||||
| chr12:79934822-79935397 | Common:1; Rare:209 | ||||
| chr12:80936539-80936643 | Rare:23 |