| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98508564-98508674 | Common:1; Rare:27 | ||||
| chr12:98509079-98509316 | Common:1; Rare:45 | ||||
| chr12:98533795-98534014 | Common:1; Rare:69; Clinvar:5; Clinvar (benign):5 | ||||
| chr12:98593005-98593065 | Common:1; Rare:17 | ||||
| chr12:100141979-100142307 | Common:4; Rare:68 | ||||
| chr12:100266459-100266554 | Rare:16 | ||||
| chr12:101052229-101052410 | Common:3; Rare:28 | ||||
| chr12:101146027-101146189 | Common:5; Rare:48 | ||||
| chr12:101608130-101608162 | Rare:8 | ||||
| chr12:101608453-101608666 | Rare:36 | ||||
| chr12:101878323-101878446 | Common:2; Rare:25 | ||||
| chr12:101878688-101878819 | Common:2; Rare:24 | ||||
| chr12:102061249-102061293 | Rare:16 | ||||
| chr12:102121067-102121197 | Rare:20 | ||||
| chr12:102539965-102540170 | Rare:39 |