| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:27523989-27524270 | Rare:66 | ||||
| chr12:27710705-27710936 | Common:2; Rare:102 | ||||
| chr12:28190371-28190506 | Common:1; Rare:42 | ||||
| chr12:30695860-30695979 | Common:1; Rare:30 | ||||
| chr12:30754762-30755081 | Common:1; Rare:130 | ||||
| chr12:31073725-31073892 | Common:7; Rare:60 | ||||
| chr12:31074100-31074271 | Common:1; Rare:33 | ||||
| chr12:31324104-31324335 | Rare:47 | ||||
| chr12:31326078-31326456 | Common:4; Rare:128 | ||||
| chr12:31729010-31729267 | Rare:74 | ||||
| chr12:31959262-31959482 | Common:2; Rare:70 | ||||
| chr12:32399637-32399907 | Common:2; Rare:78 | ||||
| chr12:32679128-32679332 | Rare:82; Clinvar (benign):1 | ||||
| chr12:32755867-32755997 | Rare:49 | ||||
| chr12:38905575-38905700 | Common:3; Rare:34 |