| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121804527-121804928 | Rare:101 | ||||
| chr12:121888444-121888949 | Common:3; Rare:138 | ||||
| chr12:121889016-121889207 | Rare:38 | ||||
| chr12:122021800-122022163 | Common:9; Rare:110 | ||||
| chr12:122078520-122078891 | Common:4; Rare:123 | ||||
| chr12:122225722-122225891 | Rare:59 | ||||
| chr12:122225893-122226074 | Rare:96; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:122226131-122226499 | Common:3; Rare:151 | ||||
| chr12:122266001-122266109 | Common:1; Rare:28 | ||||
| chr12:122266265-122266667 | Common:3; Rare:137 | ||||
| chr12:122266757-122267069 | Common:3; Rare:48 | ||||
| chr12:122399554-122399749 | Rare:31 | ||||
| chr12:122422146-122422298 | Rare:36 | ||||
| chr12:122422378-122422794 | Common:3; Rare:133 | ||||
| chr12:122500231-122500293 | Rare:9 |