| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:100475170-100475570 | Common:2; Rare:132 | ||||
| chr12:100534720-100535251 | Common:6; Rare:261; Clinvar:9; Clinvar (benign):3 | ||||
| chr12:101599743-101600370 | Common:9; Rare:177 | ||||
| chr12:101608230-101608710 | Common:2; Rare:147 | ||||
| chr12:101618340-101618782 | Common:6; Rare:154 | ||||
| chr12:101713350-101713610 | Common:3; Rare:40 | ||||
| chr12:102885220-102885660 | Common:6; Rare:157 | ||||
| chr12:102894471-102895090 | Common:2; Rare:208; Clinvar:20; Clinvar (benign):3; Clinvar (pathogenic):32 | ||||
| chr12:102898820-102899340 | Common:2; Rare:158 | ||||
| chr12:103931990-103932520 | Common:7; Rare:166 | ||||
| chr12:104265641-104265857 | Common:2; Rare:47 | ||||
| chr12:106138730-106139300 | Common:6; Rare:265 | ||||
| chr12:106274840-106275160 | Common:2; Rare:54 | ||||
| chr12:107682088-107682266 | Common:1; Rare:59 | ||||
| chr12:108689760-108690230 | Rare:176 |