| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105236068-105236403 | Common:3; Rare:148 | ||||
| chr12:105330241-105330899 | Common:4; Rare:179 | ||||
| chr12:106247447-106247536 | Common:2; Rare:22 | ||||
| chr12:106247868-106248113 | Common:1; Rare:68 | ||||
| chr12:106301819-106301979 | Common:1; Rare:32 | ||||
| chr12:106302435-106302857 | Common:6; Rare:104 | ||||
| chr12:106357637-106357838 | Common:3; Rare:45; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106357921-106358215 | Common:4; Rare:119 | ||||
| chr12:106358524-106358566 | Common:1; Rare:5 | ||||
| chr12:106773992-106774400 | Common:3; Rare:104 | ||||
| chr12:106774484-106774762 | Common:2; Rare:80 | ||||
| chr12:106774865-106774947 | Rare:39 | ||||
| chr12:106955430-106956104 | Common:6; Rare:242 | ||||
| chr12:106956122-106956284 | Rare:45 | ||||
| chr12:106956568-106956948 | Common:1; Rare:60 |