| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6943856-6944172 | Common:14; Rare:333; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6959222-6959340 | Rare:25 | ||||
| chr12:6970612-6970977 | Common:4; Rare:117; Clinvar (benign):1 | ||||
| chr12:7018430-7018563 | Common:1; Rare:46 | ||||
| chr12:7091859-7092050 | Rare:48 | ||||
| chr12:7108375-7108657 | Common:2; Rare:90 | ||||
| chr12:7130250-7130401 | Common:5; Rare:40 | ||||
| chr12:7189519-7189731 | Rare:72; Clinvar:4 | ||||
| chr12:8662629-8662837 | Common:4; Rare:48 | ||||
| chr12:8697772-8698092 | Common:2; Rare:122 | ||||
| chr12:8914359-8914813 | Common:6; Rare:134 | ||||
| chr12:8949574-8950164 | Common:4; Rare:136 | ||||
| chr12:9115762-9116291 | Common:3; Rare:117 | ||||
| chr12:9869352-9869496 | Common:1; Rare:23 | ||||
| chr12:10212237-10212527 | Rare:80 |