| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:131950266-131950368 | Rare:39 | ||||
| chr12:132083946-132084403 | Common:7; Rare:125 | ||||
| chr12:132143761-132143948 | Common:1; Rare:78 | ||||
| chr12:132144219-132144634 | Common:3; Rare:157 | ||||
| chr12:132275215-132275361 | Common:1; Rare:31 | ||||
| chr12:132489798-132490249 | Common:6; Rare:139 | ||||
| chr12:132506788-132507068 | Common:2; Rare:74 | ||||
| chr12:132559876-132560097 | Rare:73 | ||||
| chr12:132560538-132560648 | Rare:33 | ||||
| chr12:132686785-132687008 | Rare:65 | ||||
| chr12:132687086-132687158 | Rare:19 | ||||
| chr12:132687249-132687694 | Common:4; Rare:164; Clinvar:14; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr12:132687932-132687993 | Rare:8 | ||||
| chr12:132710475-132710916 | Common:5; Rare:157 | ||||
| chr12:132711213-132711493 | Common:3; Rare:62 |