| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123602028-123602174 | Common:3; Rare:55 | ||||
| chr12:123633620-123633851 | Common:1; Rare:108; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972557-123972905 | Common:6; Rare:119 | ||||
| chr12:124388794-124388934 | Common:3; Rare:42 | ||||
| chr12:124422614-124422808 | Common:2; Rare:51 | ||||
| chr12:124423035-124423334 | Common:2; Rare:74 | ||||
| chr12:124914558-124915021 | Common:9; Rare:183 | ||||
| chr12:124917166-124917370 | Rare:46 | ||||
| chr12:130871735-130872110 | Common:4; Rare:156 | ||||
| chr12:131949624-131949989 | Common:2; Rare:116 | ||||
| chr12:132687356-132687713 | Common:4; Rare:125; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:132710751-132710987 | Common:3; Rare:81 | ||||
| chr12:132887551-132887834 | Rare:82 | ||||
| chr12:132956276-132956431 | Common:1; Rare:31 | ||||
| chr12:133037209-133037536 | Common:4; Rare:66 |