| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2796930-2797282 | Rare:83 | ||||
| chr12:2812607-2812713 | Common:1; Rare:34 | ||||
| chr12:2877022-2877252 | Rare:67 | ||||
| chr12:2959843-2959960 | Common:1; Rare:31 | ||||
| chr12:3077280-3077428 | Common:4; Rare:67 | ||||
| chr12:4538449-4538784 | Rare:71 | ||||
| chr12:4648994-4649139 | Common:1; Rare:44 | ||||
| chr12:6375346-6375519 | Common:1; Rare:27; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6451809-6452120 | Common:4; Rare:59 | ||||
| chr12:6493240-6493386 | Common:5; Rare:41 | ||||
| chr12:6493826-6494001 | Common:2; Rare:60 | ||||
| chr12:6534616-6534860 | Common:3; Rare:99 | ||||
| chr12:6568255-6568382 | Rare:48 | ||||
| chr12:6606636-6606971 | Rare:114 | ||||
| chr12:6635938-6636079 | Common:2; Rare:40 |