| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32680118-32680518 | Common:4; Rare:71 | ||||
| chr12:32754950-32755480 | Common:6; Rare:480; Clinvar:12; Clinvar (benign):11; Clinvar (pathogenic):6 | ||||
| chr12:32755420-32755660 | Common:1; Rare:89; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr12:32755797-32756140 | Common:3; Rare:410 | ||||
| chr12:32756187-32756587 | Common:1; Rare:77 | ||||
| chr12:32896714-32897138 | Common:20; Rare:612; Clinvar:23; Clinvar (benign):20 | ||||
| chr12:32897095-32897270 | Common:1; Rare:56 | ||||
| chr12:33438709-33439352 | Common:14; Rare:460 | ||||
| chr12:33439468-33440230 | Common:10; Rare:362 | ||||
| chr12:33440250-33440650 | Common:1; Rare:73 | ||||
| chr12:34022130-34022587 | Common:17; Rare:498 | ||||
| chr12:38904770-38905326 | Common:3; Rare:192 | ||||
| chr12:38905507-38906173 | Common:30; Rare:470 | ||||
| chr12:38906409-38906994 | Common:7; Rare:296 | ||||
| chr12:39442138-39443089 | Common:5; Rare:335; Clinvar:1; Clinvar (benign):2 |