| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73458520-73458849 | Common:5; Rare:83 | ||||
| chr14:73567581-73567658 | Rare:22 | ||||
| chr14:73567920-73568128 | Rare:57 | ||||
| chr14:73568967-73569292 | Rare:71 | ||||
| chr14:73644893-73645036 | Common:2; Rare:40; Clinvar:2 | ||||
| chr14:73755014-73755271 | Rare:56 | ||||
| chr14:73787116-73787379 | Common:2; Rare:92 | ||||
| chr14:73790061-73790323 | Common:2; Rare:44 | ||||
| chr14:73790360-73790382 | |||||
| chr14:73851733-73851974 | Common:4; Rare:82 | ||||
| chr14:73950057-73950333 | Common:6; Rare:120; Clinvar (benign):4 | ||||
| chr14:74019248-74019436 | Common:1; Rare:74 | ||||
| chr14:74493225-74493778 | Common:4; Rare:177; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74611600-74611777 | Rare:64; Clinvar:2 | ||||
| chr14:74713049-74713200 | Rare:87 |