| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98593461-98593772 | Common:3; Rare:196; Clinvar:8; Clinvar (benign):8 | ||||
| chr12:98644536-98644839 | Common:6; Rare:162 | ||||
| chr12:98644912-98645300 | Common:6; Rare:209 | ||||
| chr12:100142298-100142539 | Rare:64 | ||||
| chr12:100199890-100200340 | Common:3; Rare:97 | ||||
| chr12:100200707-100200857 | Rare:88 | ||||
| chr12:100266604-100266880 | Common:2; Rare:95 | ||||
| chr12:100267013-100267444 | Common:4; Rare:350 | ||||
| chr12:100573507-100573804 | Rare:91 | ||||
| chr12:101407639-101408100 | Common:6; Rare:235 | ||||
| chr12:101697428-101697939 | Common:8; Rare:327 | ||||
| chr12:101877203-101877402 | Common:3; Rare:44 | ||||
| chr12:101877437-101877795 | Common:8; Rare:168 | ||||
| chr12:102061926-102062179 | Common:1; Rare:141 | ||||
| chr12:102120033-102120266 | Rare:181 |