| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2890651-2890941 | Common:1; Rare:124 | ||||
| chr12:2959804-2959940 | Common:1; Rare:38 | ||||
| chr12:3077267-3077434 | Common:5; Rare:74 | ||||
| chr12:3753088-3753275 | Common:2; Rare:46 | ||||
| chr12:3873070-3873182 | Rare:28 | ||||
| chr12:3873359-3873515 | Common:1; Rare:36 | ||||
| chr12:4320943-4321266 | Common:5; Rare:125 | ||||
| chr12:4538431-4538947 | Common:3; Rare:120 | ||||
| chr12:4649030-4649174 | Common:1; Rare:52; Clinvar (benign):2 | ||||
| chr12:6200005-6200505 | Common:4; Rare:150 | ||||
| chr12:6201261-6201323 | Common:1; Rare:17 | ||||
| chr12:6342002-6342123 | Rare:28; Clinvar (benign):1 | ||||
| chr12:6470643-6470839 | Common:1; Rare:56 | ||||
| chr12:6493175-6493502 | Common:8; Rare:99 | ||||
| chr12:6493656-6494146 | Common:2; Rare:131 |