| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123533712-123533720 | Rare:1 | ||||
| chr12:123584314-123584813 | Common:9; Rare:167 | ||||
| chr12:123601991-123602204 | Common:3; Rare:75 | ||||
| chr12:123633545-123633868 | Common:2; Rare:157; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123712212-123712409 | Common:3; Rare:80; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:123972866-123973350 | Common:2; Rare:150 | ||||
| chr12:124567435-124567618 | Rare:48 | ||||
| chr12:124786440-124786789 | Common:3; Rare:95 | ||||
| chr12:124863823-124864027 | Common:1; Rare:52 | ||||
| chr12:124914589-124914967 | Common:7; Rare:146 | ||||
| chr12:124993836-124993980 | Common:1; Rare:38 | ||||
| chr12:125065301-125065504 | Common:2; Rare:71 | ||||
| chr12:125186235-125186387 | Rare:57 | ||||
| chr12:128823920-128824131 | Common:2; Rare:74 | ||||
| chr12:130871755-130872142 | Common:4; Rare:155 |