| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:29783514-29783788 | Common:8; Rare:82 | ||||
| chr12:30695810-30695923 | Common:1; Rare:35 | ||||
| chr12:30754749-30755167 | Common:4; Rare:156 | ||||
| chr12:31073735-31073902 | Common:8; Rare:61 | ||||
| chr12:31074079-31074271 | Common:1; Rare:38 | ||||
| chr12:31659151-31659229 | Common:1; Rare:29 | ||||
| chr12:31728826-31729351 | Common:3; Rare:150 | ||||
| chr12:31959124-31959483 | Common:3; Rare:99 | ||||
| chr12:31959540-31959873 | Common:2; Rare:116 | ||||
| chr12:32107069-32107319 | Common:2; Rare:56 | ||||
| chr12:32399842-32399885 | Rare:16 | ||||
| chr12:32755471-32755543 | Rare:22; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:32755875-32756028 | Common:1; Rare:51 | ||||
| chr12:32896760-32896990 | Common:2; Rare:78; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:38905491-38905814 | Common:6; Rare:95 |