| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35826101-35826480 | Common:1; Rare:94 | ||||
| chr14:36320212-36320772 | Common:5; Rare:167 | ||||
| chr14:36477591-36477630 | Rare:9 | ||||
| chr14:36513378-36514082 | Common:1; Rare:158 | ||||
| chr14:36519717-36519917 | Common:1; Rare:39 | ||||
| chr14:36520104-36520657 | Common:8; Rare:142; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr14:36520660-36521179 | Common:3; Rare:125 | ||||
| chr14:36521183-36521265 | Common:1; Rare:23 | ||||
| chr14:37172036-37172157 | Rare:39 | ||||
| chr14:37595338-37595645 | Common:1; Rare:89 | ||||
| chr14:37595998-37596058 | Common:1; Rare:7 | ||||
| chr14:38256051-38256228 | Common:1; Rare:47 | ||||
| chr14:38256376-38256642 | Common:1; Rare:49 | ||||
| chr14:39113986-39114389 | Common:2; Rare:117 | ||||
| chr14:39170172-39170471 | Common:3; Rare:77 |