| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122021769-122022045 | Common:9; Rare:74 | ||||
| chr12:122078322-122078896 | Common:5; Rare:183 | ||||
| chr12:122079083-122079199 | Rare:19 | ||||
| chr12:122203389-122203763 | Common:1; Rare:137 | ||||
| chr12:122225576-122225744 | Common:1; Rare:44 | ||||
| chr12:122225747-122225842 | Rare:31 | ||||
| chr12:122225899-122226499 | Common:3; Rare:286; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:122265806-122265882 | Rare:17 | ||||
| chr12:122266001-122266122 | Common:1; Rare:32 | ||||
| chr12:122266306-122266705 | Common:3; Rare:126 | ||||
| chr12:122266987-122267068 | Rare:13 | ||||
| chr12:122399970-122400155 | Rare:38 | ||||
| chr12:122400469-122400759 | Common:1; Rare:51 | ||||
| chr12:122421878-122422280 | Rare:94 | ||||
| chr12:122422343-122422838 | Common:4; Rare:155 |