| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:54053777-54053872 | Rare:11 | ||||
| chr12:54259517-54259675 | Rare:32 | ||||
| chr12:54403909-54404241 | Common:3; Rare:80 | ||||
| chr12:54419079-54419820 | Common:1; Rare:178 | ||||
| chr12:54561359-54561481 | Common:1; Rare:23 | ||||
| chr12:55712066-55712295 | Common:7; Rare:64; Clinvar (benign):1 | ||||
| chr12:55715984-55716195 | Common:2; Rare:95 | ||||
| chr12:55716361-55716600 | Common:3; Rare:64 | ||||
| chr12:55720210-55720494 | Common:4; Rare:38; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:55728939-55729225 | Rare:62 | ||||
| chr12:55729655-55729827 | Rare:42 | ||||
| chr12:55829501-55829793 | Rare:92 | ||||
| chr12:55830753-55830984 | Common:2; Rare:68 | ||||
| chr12:55931953-55932095 | Rare:39 | ||||
| chr12:55966685-55966880 | Rare:52 |