| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:103965705-103965910 | Common:2; Rare:53 | ||||
| chr12:104064435-104064560 | Rare:30 | ||||
| chr12:106247970-106248050 | Rare:24 | ||||
| chr12:106955648-106955978 | Common:2; Rare:115 | ||||
| chr12:109477275-109477437 | Common:3; Rare:60 | ||||
| chr12:109573481-109573858 | Common:3; Rare:109; Clinvar:6; Clinvar (benign):5 | ||||
| chr12:110502069-110502188 | Common:1; Rare:45 | ||||
| chr12:110613988-110614168 | Rare:54; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:111685790-111686110 | Rare:124 | ||||
| chr12:111841915-111842257 | Common:2; Rare:95 | ||||
| chr12:112013129-112013487 | Common:1; Rare:130 | ||||
| chr12:113185440-113185769 | Common:8; Rare:117 | ||||
| chr12:118135955-118136265 | Common:2; Rare:91 | ||||
| chr12:120116740-120116916 | Rare:51 | ||||
| chr12:120201084-120201349 | Common:2; Rare:84 |