| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103522806-103523063 | Common:1; Rare:79 | ||||
| chr14:103528946-103529289 | Common:1; Rare:92 | ||||
| chr14:103561363-103561639 | Common:1; Rare:58 | ||||
| chr14:103561843-103562047 | Common:4; Rare:79 | ||||
| chr14:103562216-103562498 | Common:1; Rare:117 | ||||
| chr14:103562571-103563312 | Common:11; Rare:307; Clinvar:1; Clinvar (benign):9 | ||||
| chr14:103628641-103628985 | Common:3; Rare:68 | ||||
| chr14:103628990-103629328 | Common:1; Rare:123 | ||||
| chr14:103629385-103629497 | Common:2; Rare:38 | ||||
| chr14:103629539-103629813 | Common:6; Rare:80 | ||||
| chr14:103673177-103673188 | Rare:1 | ||||
| chr14:103715352-103715919 | Common:1; Rare:194 | ||||
| chr14:103716261-103716394 | Common:1; Rare:25 | ||||
| chr14:103847187-103847392 | Common:1; Rare:59 | ||||
| chr14:103847482-103847877 | Common:5; Rare:157 |