| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20683498-20683666 | Common:1; Rare:44 | ||||
| chr14:20683687-20684072 | Common:10; Rare:134 | ||||
| chr14:20684093-20684322 | Common:6; Rare:65; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:20684373-20684818 | Common:5; Rare:85; Clinvar:2; Clinvar (benign):5 | ||||
| chr14:20685069-20685259 | Common:2; Rare:29 | ||||
| chr14:20989615-20990057 | Common:8; Rare:112 | ||||
| chr14:20990308-20990482 | Common:1; Rare:64 | ||||
| chr14:21041784-21041937 | Rare:38 | ||||
| chr14:21042226-21042406 | Common:1; Rare:31 | ||||
| chr14:21070285-21070415 | Common:1; Rare:29 | ||||
| chr14:21070725-21070746 | Rare:6 | ||||
| chr14:21098277-21098363 | Rare:15 | ||||
| chr14:21098473-21098861 | Common:1; Rare:85 | ||||
| chr14:21103582-21103916 | Common:2; Rare:74 | ||||
| chr14:21103944-21104176 | Common:2; Rare:56 |