| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:100266724-100266938 | Rare:67 | ||||
| chr12:100266945-100267474 | Common:4; Rare:220 | ||||
| chr12:100267868-100267973 | Rare:20 | ||||
| chr12:100573469-100573776 | Rare:89 | ||||
| chr12:100573886-100573945 | Common:1; Rare:21 | ||||
| chr12:100573966-100574161 | Common:4; Rare:40 | ||||
| chr12:101279938-101280227 | Common:1; Rare:82 | ||||
| chr12:101407696-101408188 | Common:3; Rare:118 | ||||
| chr12:101830604-101830676 | Common:2; Rare:26; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr12:101830765-101831189 | Common:2; Rare:135; Clinvar (benign):2 | ||||
| chr12:101877104-101877456 | Common:4; Rare:70 | ||||
| chr12:101877497-101877795 | Common:5; Rare:77 | ||||
| chr12:102061710-102061826 | Common:1; Rare:28 | ||||
| chr12:102061903-102062194 | Common:1; Rare:83 | ||||
| chr12:102119941-102120353 | Common:1; Rare:139 |