| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:131928996-131929354 | Common:10; Rare:111; Clinvar:1 | ||||
| chr12:131940393-131940442 | Common:2; Rare:11 | ||||
| chr12:131949615-131950098 | Common:2; Rare:157 | ||||
| chr12:131950256-131950351 | Rare:33 | ||||
| chr12:132084015-132084523 | Common:7; Rare:147 | ||||
| chr12:132084867-132085151 | Common:2; Rare:59 | ||||
| chr12:132143908-132143950 | Rare:17 | ||||
| chr12:132144246-132144551 | Common:3; Rare:123 | ||||
| chr12:132489828-132490279 | Common:5; Rare:134 | ||||
| chr12:132559815-132560132 | Rare:91 | ||||
| chr12:132560547-132560662 | Common:1; Rare:31 | ||||
| chr12:132686832-132687128 | Rare:82 | ||||
| chr12:132687226-132687705 | Common:5; Rare:173; Clinvar:15; Clinvar (benign):15; Clinvar (pathogenic):1 | ||||
| chr12:132687761-132687873 | Rare:30 | ||||
| chr12:132687932-132687991 | Rare:8 |