| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:91510251-91510605 | Common:1; Rare:112 | ||||
| chr14:92040026-92040192 | Common:2; Rare:46; Clinvar (benign):1 | ||||
| chr14:92121643-92121990 | Common:5; Rare:115 | ||||
| chr14:93184822-93185008 | Rare:63 | ||||
| chr14:93206985-93207333 | Common:3; Rare:174 | ||||
| chr14:93976527-93976674 | Rare:31 | ||||
| chr14:93976707-93976850 | Rare:26 | ||||
| chr14:94081133-94081341 | Common:4; Rare:69 | ||||
| chr14:95157416-95157742 | Common:4; Rare:118 | ||||
| chr14:95534605-95534695 | Rare:29 | ||||
| chr14:96363286-96363552 | Common:1; Rare:89 | ||||
| chr14:96502268-96502564 | Common:1; Rare:130 | ||||
| chr14:100376259-100376494 | Common:3; Rare:77 | ||||
| chr14:102139671-102139936 | Rare:92 | ||||
| chr14:102362847-102363103 | Rare:114 |