| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6970612-6970977 | Common:4; Rare:117; Clinvar (benign):1 | ||||
| chr12:7018468-7018584 | Common:1; Rare:30 | ||||
| chr12:7108475-7108696 | Common:1; Rare:61 | ||||
| chr12:7189549-7189731 | Rare:66; Clinvar:4 | ||||
| chr12:8662651-8662937 | Common:4; Rare:62 | ||||
| chr12:8697794-8698023 | Rare:94 | ||||
| chr12:8914392-8914714 | Common:6; Rare:97 | ||||
| chr12:10613494-10613675 | Common:1; Rare:75 | ||||
| chr12:11171565-11171722 | Common:2; Rare:53 | ||||
| chr12:12357004-12357212 | Common:4; Rare:104 | ||||
| chr12:12561143-12561246 | Common:1; Rare:17 | ||||
| chr12:12611765-12612164 | Common:3; Rare:116 | ||||
| chr12:12725642-12725924 | Common:2; Rare:62 | ||||
| chr12:12891272-12891567 | Common:1; Rare:60 | ||||
| chr12:13000196-13000473 | Common:2; Rare:90 |