| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98593409-98593749 | Common:2; Rare:121; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:98644697-98644870 | Common:3; Rare:55 | ||||
| chr12:98644935-98645341 | Common:2; Rare:120 | ||||
| chr12:99154640-99155199 | Common:1; Rare:174 | ||||
| chr12:99984159-99984594 | Common:3; Rare:150 | ||||
| chr12:99984600-99985050 | Common:3; Rare:141 | ||||
| chr12:100142202-100142603 | Common:2; Rare:159 | ||||
| chr12:100142826-100143014 | Common:2; Rare:73 | ||||
| chr12:100200688-100200873 | Common:1; Rare:61 | ||||
| chr12:100266939-100267290 | Common:2; Rare:168 | ||||
| chr12:100573410-100573860 | Rare:123 | ||||
| chr12:101279997-101280374 | Common:1; Rare:111 | ||||
| chr12:101407703-101408092 | Common:3; Rare:98 | ||||
| chr12:101697060-101697330 | Common:3; Rare:38 | ||||
| chr12:101697425-101697685 | Common:2; Rare:74 |