| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73568910-73569292 | Common:1; Rare:76 | ||||
| chr14:73787109-73787371 | Common:3; Rare:91 | ||||
| chr14:73886765-73886893 | Common:2; Rare:44 | ||||
| chr14:73950074-73950330 | Common:6; Rare:105; Clinvar (benign):4 | ||||
| chr14:74019248-74019467 | Common:1; Rare:82 | ||||
| chr14:74084369-74084657 | Common:4; Rare:78 | ||||
| chr14:74302905-74303078 | Common:1; Rare:74; Clinvar (benign):1 | ||||
| chr14:74493221-74493776 | Common:4; Rare:179; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74713015-74713207 | Common:1; Rare:108 | ||||
| chr14:74763070-74763425 | Rare:102 | ||||
| chr14:74881801-74882007 | Common:1; Rare:91 | ||||
| chr14:75002698-75002967 | Common:1; Rare:89; Clinvar:2 | ||||
| chr14:75127008-75127128 | Rare:38 | ||||
| chr14:75176550-75176898 | Common:1; Rare:97 | ||||
| chr14:75660789-75661330 | Common:4; Rare:132 |