| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:131796261-131796381 | Rare:34 | ||||
| chr12:131828270-131828465 | Common:3; Rare:72 | ||||
| chr12:131894383-131894736 | Common:3; Rare:111 | ||||
| chr12:131928817-131929346 | Common:11; Rare:158; Clinvar:1 | ||||
| chr12:131929672-131929828 | Rare:68; Clinvar (benign):3 | ||||
| chr12:131949608-131950117 | Common:2; Rare:167 | ||||
| chr12:131950262-131950343 | Rare:28 | ||||
| chr12:132084034-132084502 | Common:7; Rare:141 | ||||
| chr12:132084855-132085118 | Common:2; Rare:55 | ||||
| chr12:132143909-132143948 | Rare:15 | ||||
| chr12:132144222-132144552 | Common:3; Rare:130 | ||||
| chr12:132275213-132275423 | Common:3; Rare:47 | ||||
| chr12:132489770-132490229 | Common:6; Rare:137 | ||||
| chr12:132559876-132560129 | Rare:80 | ||||
| chr12:132560515-132560691 | Common:1; Rare:44 |