| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110449812-110449907 | Rare:14 | ||||
| chr12:110450240-110450508 | Common:2; Rare:89 | ||||
| chr12:110468123-110468903 | Common:3; Rare:242 | ||||
| chr12:110469200-110469395 | Common:1; Rare:30 | ||||
| chr12:110501994-110502371 | Common:1; Rare:144 | ||||
| chr12:110582657-110582839 | Common:1; Rare:49 | ||||
| chr12:110583221-110583531 | Rare:88 | ||||
| chr12:110613900-110614212 | Rare:89; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:110688983-110689529 | Common:1; Rare:130 | ||||
| chr12:110689546-110689672 | Rare:25 | ||||
| chr12:110689728-110690083 | Common:1; Rare:54 | ||||
| chr12:110742829-110743251 | Common:3; Rare:143 | ||||
| chr12:111368980-111369265 | Common:1; Rare:76 | ||||
| chr12:111405314-111405477 | Common:1; Rare:30 | ||||
| chr12:111405744-111406084 | Rare:106 |