| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:91060526-91060706 | Rare:62 | ||||
| chr14:91060826-91061198 | Common:1; Rare:86 | ||||
| chr14:91113973-91114185 | Common:1; Rare:62 | ||||
| chr14:91114244-91114744 | Common:2; Rare:84 | ||||
| chr14:91243568-91244101 | Common:2; Rare:93 | ||||
| chr14:91253425-91253559 | Common:1; Rare:42 | ||||
| chr14:91415989-91416547 | Common:2; Rare:108 | ||||
| chr14:91416847-91416950 | Common:1; Rare:27 | ||||
| chr14:91417536-91417692 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr14:91417789-91418276 | Common:3; Rare:142 | ||||
| chr14:91509178-91509261 | Rare:19 | ||||
| chr14:91509278-91509294 | Rare:1 | ||||
| chr14:91510202-91510929 | Common:3; Rare:238 | ||||
| chr14:92039540-92039594 | Common:2; Rare:16; Clinvar (benign):2 | ||||
| chr14:92039954-92040292 | Common:4; Rare:90; Clinvar:3; Clinvar (benign):2 |