| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:76764010-76764281 | Common:2; Rare:112 | ||||
| chr12:79934771-79935363 | Common:1; Rare:212 | ||||
| chr12:80707181-80707559 | Common:2; Rare:63 | ||||
| chr12:80707590-80708257 | Common:1; Rare:216; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:80937684-80937799 | Common:1; Rare:35 | ||||
| chr12:82358322-82358556 | Rare:110 | ||||
| chr12:82358700-82358897 | Common:3; Rare:105 | ||||
| chr12:88035433-88035589 | Common:1; Rare:48 | ||||
| chr12:88142032-88142382 | Rare:96; Clinvar:3 | ||||
| chr12:88580440-88580551 | Common:1; Rare:40 | ||||
| chr12:89352464-89352714 | Rare:75 | ||||
| chr12:89524557-89524594 | Rare:14 | ||||
| chr12:89524755-89524874 | Common:1; Rare:21 | ||||
| chr12:89525992-89526282 | Rare:83 | ||||
| chr12:89708819-89709106 | Common:1; Rare:110 |