| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:132687322-132687662 | Common:2; Rare:121; Clinvar:2; Clinvar (benign):8 | ||||
| chr12:132747860-132748160 | Common:5; Rare:119; Clinvar:1 | ||||
| chr12:132761814-132762185 | Common:3; Rare:128 | ||||
| chr12:132829018-132829228 | Rare:95 | ||||
| chr12:132854046-132854213 | Common:1; Rare:40 | ||||
| chr12:132887550-132887766 | Rare:68 | ||||
| chr12:132956243-132956370 | Common:1; Rare:32 | ||||
| chr12:132986242-132986446 | Rare:47 | ||||
| chr12:133037182-133037563 | Common:5; Rare:80 | ||||
| chr12:133039911-133040128 | Common:1; Rare:28 | ||||
| chr12:133080217-133080453 | Common:6; Rare:69 | ||||
| chr12:133130239-133130361 | Common:1; Rare:29 | ||||
| chr12:133130391-133130633 | Common:5; Rare:81 | ||||
| chr13:19633811-19633854 | Rare:14 | ||||
| chr13:19633893-19633959 | Rare:25 |