| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:30754762-30755100 | Common:1; Rare:134 | ||||
| chr12:31073754-31073902 | Common:8; Rare:56 | ||||
| chr12:31074085-31074271 | Common:1; Rare:37 | ||||
| chr12:31324087-31324226 | Rare:37 | ||||
| chr12:31326078-31326451 | Common:4; Rare:128 | ||||
| chr12:31729010-31729308 | Common:1; Rare:93 | ||||
| chr12:31958981-31959234 | Common:1; Rare:55 | ||||
| chr12:31959262-31959488 | Common:2; Rare:73 | ||||
| chr12:32106627-32106895 | Common:4; Rare:73 | ||||
| chr12:32399235-32399577 | Common:4; Rare:93 | ||||
| chr12:32399827-32399939 | Common:1; Rare:34 | ||||
| chr12:32755853-32756028 | Common:1; Rare:63 | ||||
| chr12:32896738-32896999 | Common:4; Rare:85; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:38905526-38905733 | Common:3; Rare:57 | ||||
| chr12:39619785-39619932 | Common:1; Rare:27 |