| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:91416204-91416604 | Rare:95 | ||||
| chr14:91416678-91417078 | Common:4; Rare:121; Clinvar (benign):1 | ||||
| chr14:91417159-91417658 | Common:5; Rare:228; Clinvar (benign):2 | ||||
| chr14:91417695-91418171 | Common:12; Rare:400 | ||||
| chr14:91418099-91418499 | Common:5; Rare:142 | ||||
| chr14:91509179-91509914 | Common:6; Rare:666 | ||||
| chr14:91510190-91510720 | Common:6; Rare:827 | ||||
| chr14:91510740-91510963 | Common:1; Rare:104 | ||||
| chr14:91510940-91511392 | Common:4; Rare:134 | ||||
| chr14:91835874-91836840 | Common:98; Rare:686 | ||||
| chr14:92039436-92040288 | Common:28; Rare:687; Clinvar:25; Clinvar (benign):19 | ||||
| chr14:92040379-92040497 | Rare:33 | ||||
| chr14:92040615-92041050 | Common:6; Rare:122 | ||||
| chr14:92106078-92106868 | Common:18; Rare:708 | ||||
| chr14:92121149-92121549 | Common:8; Rare:79 |