| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:28190360-28190545 | Common:1; Rare:57 | ||||
| chr12:28190906-28191224 | Common:1; Rare:68 | ||||
| chr12:29343257-29343490 | Common:1; Rare:64 | ||||
| chr12:29381136-29381304 | Common:2; Rare:58 | ||||
| chr12:30695803-30696002 | Common:2; Rare:54 | ||||
| chr12:30754735-30755064 | Common:1; Rare:127 | ||||
| chr12:31073732-31073892 | Common:7; Rare:59 | ||||
| chr12:31326084-31326423 | Common:3; Rare:99 | ||||
| chr12:31728993-31729303 | Common:1; Rare:101 | ||||
| chr12:31959262-31959488 | Common:2; Rare:73 | ||||
| chr12:32534237-32534389 | Common:2; Rare:31 | ||||
| chr12:32740323-32740449 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr12:32755867-32756011 | Rare:52 | ||||
| chr12:32896760-32896990 | Common:2; Rare:78; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:38905560-38905804 | Common:5; Rare:67 |