| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:74537580-74538008 | Common:7; Rare:499 | ||||
| chr12:74537946-74538346 | Rare:124 | ||||
| chr12:75329950-75330565 | Common:4; Rare:357 | ||||
| chr12:75390804-75391254 | Common:7; Rare:837 | ||||
| chr12:75480454-75480854 | Rare:239 | ||||
| chr12:75511361-75511870 | Common:2; Rare:422 | ||||
| chr12:76031328-76031940 | Common:5; Rare:582 | ||||
| chr12:76032090-76032766 | Common:6; Rare:254 | ||||
| chr12:76033204-76033739 | Common:7; Rare:129 | ||||
| chr12:76083710-76084240 | Common:2; Rare:497 | ||||
| chr12:76084382-76085655 | Common:31; Rare:703 | ||||
| chr12:76347840-76348260 | Common:1; Rare:175; Clinvar (pathogenic):6 | ||||
| chr12:76348290-76348599 | Common:10; Rare:497; Clinvar:22; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr12:76348516-76348916 | Common:1; Rare:82 | ||||
| chr12:76558740-76559340 | Common:3; Rare:111 |