| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122980590-122980782 | Common:1; Rare:69 | ||||
| chr12:123233087-123233486 | Common:2; Rare:130; Clinvar:1 | ||||
| chr12:123364820-123364974 | Common:2; Rare:61 | ||||
| chr12:123584317-123584616 | Common:6; Rare:103 | ||||
| chr12:123602023-123602164 | Common:3; Rare:52 | ||||
| chr12:123633620-123633851 | Common:1; Rare:108; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:125065303-125065478 | Common:2; Rare:68 | ||||
| chr12:130871937-130872122 | Common:4; Rare:75 | ||||
| chr12:131710825-131711125 | Rare:75 | ||||
| chr12:132710747-132711020 | Common:3; Rare:88 | ||||
| chr12:132828840-132829159 | Common:4; Rare:107 | ||||
| chr12:132887558-132887810 | Rare:76 | ||||
| chr12:132956280-132956423 | Common:1; Rare:28 | ||||
| chr12:132986230-132986428 | Rare:43 | ||||
| chr12:133130238-133130662 | Common:7; Rare:142 |