| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:21104518-21104720 | Common:3; Rare:37 | ||||
| chr14:21268902-21269079 | Rare:60 | ||||
| chr14:21269373-21269468 | Rare:39 | ||||
| chr14:21269740-21270022 | Common:2; Rare:95 | ||||
| chr14:21301018-21301146 | Common:1; Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:21320094-21320170 | Common:1; Rare:20; Clinvar:1 | ||||
| chr14:21383420-21383761 | Common:2; Rare:113 | ||||
| chr14:21383770-21384058 | Common:2; Rare:109 | ||||
| chr14:21384202-21384580 | Rare:115 | ||||
| chr14:21384602-21384722 | Rare:35 | ||||
| chr14:21437215-21437486 | Common:4; Rare:105 | ||||
| chr14:21437625-21437661 | Rare:8 | ||||
| chr14:21455745-21455794 | Rare:8 | ||||
| chr14:21455842-21455869 | Rare:7 | ||||
| chr14:21455987-21456355 | Common:4; Rare:98 |