| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123458083-123458229 | Common:1; Rare:36 | ||||
| chr12:123584278-123584816 | Common:9; Rare:176 | ||||
| chr12:123602006-123602204 | Common:3; Rare:70 | ||||
| chr12:123633571-123633887 | Common:2; Rare:154; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:124422636-124422808 | Common:2; Rare:44 | ||||
| chr12:124423020-124423363 | Common:2; Rare:83 | ||||
| chr12:124863596-124863777 | Common:4; Rare:53 | ||||
| chr12:124863833-124864125 | Common:1; Rare:82 | ||||
| chr12:124914026-124914193 | Common:6; Rare:69 | ||||
| chr12:124914578-124915097 | Common:9; Rare:210 | ||||
| chr12:124915262-124915376 | Rare:32 | ||||
| chr12:124917150-124917529 | Common:1; Rare:95 | ||||
| chr12:124917530-124917812 | Common:1; Rare:77 | ||||
| chr12:124980200-124980501 | Common:4; Rare:73 | ||||
| chr12:125065148-125065479 | Common:2; Rare:119 |