| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31665876-31666146 | Common:3; Rare:76 | ||||
| chr6:31958906-31959182 | Rare:83; Clinvar:8 | ||||
| chr6:32844009-32844086 | Rare:21; Clinvar:1 | ||||
| chr6:33200660-33200909 | Common:1; Rare:75 | ||||
| chr6:33271842-33272122 | Common:1; Rare:117 | ||||
| chr6:41921111-41921217 | Rare:27 | ||||
| chr6:42929232-42929494 | Common:3; Rare:65 | ||||
| chr6:43013903-43014261 | Common:1; Rare:73 | ||||
| chr6:43516893-43517106 | Common:3; Rare:84; Clinvar:2 | ||||
| chr6:43770043-43770216 | Common:4; Rare:56 | ||||
| chr6:44127369-44127629 | Common:4; Rare:73 | ||||
| chr6:49463194-49463376 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52995290-52995734 | Common:4; Rare:179 | ||||
| chr6:75284731-75285033 | Common:1; Rare:87 | ||||
| chr6:83193226-83193364 | Common:3; Rare:49 |