| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50085046-50085370 | Common:2; Rare:166 | ||||
| chr12:50111941-50112301 | Common:4; Rare:137 | ||||
| chr12:50166610-50167240 | Common:3; Rare:158 | ||||
| chr12:50167241-50167684 | Common:6; Rare:220 | ||||
| chr12:50283477-50283711 | Common:5; Rare:128 | ||||
| chr12:50400705-50401018 | Common:1; Rare:174 | ||||
| chr12:50401230-50401450 | Common:2; Rare:72 | ||||
| chr12:50504818-50505173 | Common:8; Rare:256 | ||||
| chr12:50763741-50764727 | Common:12; Rare:470 | ||||
| chr12:50924480-50924737 | Common:6; Rare:151 | ||||
| chr12:51024750-51025110 | Common:2; Rare:78 | ||||
| chr12:51026209-51026554 | Common:7; Rare:222; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:51028170-51028640 | Common:2; Rare:105 | ||||
| chr12:51028830-51029110 | Common:1; Rare:85 | ||||
| chr12:51048059-51048456 | Common:4; Rare:241 |