| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35121909-35122386 | Common:2; Rare:136 | ||||
| chr14:35122498-35122806 | Common:2; Rare:90 | ||||
| chr14:35292163-35292495 | Common:5; Rare:115; Clinvar:1 | ||||
| chr14:35403690-35404083 | Common:1; Rare:133; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:35404419-35404875 | Common:3; Rare:147; Clinvar:1; Clinvar (benign):5 | ||||
| chr14:35826306-35826497 | Common:1; Rare:56 | ||||
| chr14:35826705-35826913 | Common:1; Rare:54 | ||||
| chr14:36320607-36320811 | Common:1; Rare:53 | ||||
| chr14:37171973-37172166 | Rare:52 | ||||
| chr14:37172554-37172622 | Common:2; Rare:30 | ||||
| chr14:39103436-39103596 | Rare:43 | ||||
| chr14:39170289-39170487 | Common:2; Rare:65 | ||||
| chr14:39179068-39179473 | Common:1; Rare:113 | ||||
| chr14:39267032-39267436 | Common:2; Rare:146 | ||||
| chr14:39432379-39432641 | Common:8; Rare:89 |