| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:103587090-103587285 | Common:1; Rare:51 | ||||
| chr12:103930077-103930557 | Common:8; Rare:164 | ||||
| chr12:103965722-103965941 | Common:2; Rare:51 | ||||
| chr12:104064451-104064582 | Rare:32 | ||||
| chr12:104138134-104138377 | Common:1; Rare:58 | ||||
| chr12:104286830-104287140 | Common:3; Rare:62 | ||||
| chr12:105107612-105107818 | Common:1; Rare:96; Clinvar:1 | ||||
| chr12:105236029-105236294 | Common:2; Rare:114 | ||||
| chr12:106357500-106357819 | Common:3; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106357939-106358139 | Common:3; Rare:93 | ||||
| chr12:106774555-106774715 | Common:1; Rare:52 | ||||
| chr12:106955650-106955907 | Rare:90 | ||||
| chr12:106987040-106987277 | Common:4; Rare:69 | ||||
| chr12:107093477-107093642 | Rare:61 | ||||
| chr12:107685705-107685934 | Rare:76 |