| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103333744-103334359 | Common:6; Rare:226 | ||||
| chr14:103334625-103334844 | Common:1; Rare:98 | ||||
| chr14:103335115-103335250 | Common:3; Rare:43 | ||||
| chr14:103385168-103385541 | Common:1; Rare:129 | ||||
| chr14:103529051-103529239 | Common:1; Rare:57 | ||||
| chr14:103562556-103563285 | Common:11; Rare:303; Clinvar:1; Clinvar (benign):9 | ||||
| chr14:103628736-103628862 | Common:2; Rare:21 | ||||
| chr14:103628879-103629483 | Common:6; Rare:191 | ||||
| chr14:103629765-103630022 | Common:1; Rare:71 | ||||
| chr14:103715385-103715914 | Common:1; Rare:178 | ||||
| chr14:103847565-103847849 | Common:5; Rare:117 | ||||
| chr14:103921433-103921724 | Common:3; Rare:89 | ||||
| chr14:104689478-104689703 | Common:1; Rare:54; Clinvar (benign):1 | ||||
| chr14:104724108-104724277 | Common:3; Rare:68 | ||||
| chr14:104752532-104752657 | Rare:36 |