| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121918171-121918234 | Rare:16 | ||||
| chr12:121918392-121918642 | Common:5; Rare:53 | ||||
| chr12:122021814-122022040 | Common:9; Rare:61 | ||||
| chr12:122022076-122022334 | Common:1; Rare:79 | ||||
| chr12:122078337-122078384 | Rare:6 | ||||
| chr12:122078488-122078789 | Common:2; Rare:95 | ||||
| chr12:122225225-122225496 | Common:1; Rare:86 | ||||
| chr12:122225570-122225755 | Common:1; Rare:45 | ||||
| chr12:122225919-122226547 | Common:3; Rare:298; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:122266022-122266104 | Common:1; Rare:22 | ||||
| chr12:122266316-122266657 | Common:2; Rare:118 | ||||
| chr12:122399419-122399758 | Common:1; Rare:59 | ||||
| chr12:122399966-122400151 | Rare:38 | ||||
| chr12:122400501-122400752 | Common:1; Rare:44 | ||||
| chr12:122422139-122422293 | Rare:36 |