| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31326103-31326456 | Common:4; Rare:120 | ||||
| chr12:31728995-31729295 | Common:1; Rare:93 | ||||
| chr12:31959276-31959482 | Common:2; Rare:65 | ||||
| chr12:32399718-32399885 | Common:1; Rare:59 | ||||
| chr12:32679098-32679358 | Common:1; Rare:105; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32755861-32756036 | Common:1; Rare:63 | ||||
| chr12:32896695-32896999 | Common:4; Rare:102; Clinvar:6; Clinvar (benign):7 | ||||
| chr12:34022426-34022520 | Rare:34 | ||||
| chr12:38905548-38905810 | Common:5; Rare:75 | ||||
| chr12:38906287-38906623 | Common:2; Rare:74 | ||||
| chr12:38906713-38906924 | Common:1; Rare:45 | ||||
| chr12:39619744-39619919 | Common:1; Rare:29 | ||||
| chr12:40692317-40692575 | Common:1; Rare:81 | ||||
| chr12:40827812-40828228 | Rare:75 | ||||
| chr12:42238176-42238483 | Common:1; Rare:104 |