| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12696148-12696292 | Rare:38 | ||||
| chr12:12696634-12696763 | Rare:40 | ||||
| chr12:12717183-12717480 | Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12725625-12725983 | Common:4; Rare:82 | ||||
| chr12:13000204-13000499 | Common:2; Rare:93 | ||||
| chr12:13980573-13980657 | Rare:21 | ||||
| chr12:13980788-13980972 | Common:1; Rare:43 | ||||
| chr12:14365492-14365719 | Common:1; Rare:74 | ||||
| chr12:14384932-14385109 | Common:1; Rare:31 | ||||
| chr12:14385203-14385382 | Rare:31 | ||||
| chr12:14771124-14771235 | Rare:35 | ||||
| chr12:14774184-14774477 | Common:3; Rare:76 | ||||
| chr12:14803437-14803715 | Common:1; Rare:73 | ||||
| chr12:15221231-15221564 | Common:1; Rare:96 | ||||
| chr12:15882241-15882647 | Common:1; Rare:131 |