| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50504792-50505246 | Common:8; Rare:280 | ||||
| chr12:50763882-50764126 | Common:4; Rare:143 | ||||
| chr12:50764386-50764514 | Common:4; Rare:41 | ||||
| chr12:50924350-50924763 | Common:6; Rare:162 | ||||
| chr12:51025610-51026020 | Common:2; Rare:157 | ||||
| chr12:51026206-51026602 | Common:13; Rare:267; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:51048077-51048389 | Common:4; Rare:200 | ||||
| chr12:51083515-51083752 | Rare:145 | ||||
| chr12:51172742-51172921 | Common:5; Rare:62 | ||||
| chr12:51173043-51173291 | Rare:70 | ||||
| chr12:51217900-51218410 | Common:10; Rare:183 | ||||
| chr12:51238648-51238899 | Common:16; Rare:215 | ||||
| chr12:51239030-51239350 | Common:5; Rare:154 | ||||
| chr12:51269700-51270230 | Common:5; Rare:305 | ||||
| chr12:51951485-51951750 | Common:4; Rare:103 |