| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20683693-20684288 | Common:20; Rare:208; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:20684370-20684644 | Common:3; Rare:48; Clinvar (benign):4 | ||||
| chr14:20989620-20989714 | Common:1; Rare:28 | ||||
| chr14:20989725-20989801 | Common:4; Rare:9 | ||||
| chr14:20989815-20990050 | Common:3; Rare:68 | ||||
| chr14:21024886-21025080 | Common:1; Rare:62 | ||||
| chr14:21070294-21070389 | Common:1; Rare:24 | ||||
| chr14:21098268-21098622 | Common:1; Rare:84 | ||||
| chr14:21098678-21098844 | Rare:34 | ||||
| chr14:21103625-21103931 | Common:2; Rare:73 | ||||
| chr14:21103950-21104145 | Common:1; Rare:44 | ||||
| chr14:21104152-21104432 | Common:4; Rare:59 | ||||
| chr14:21104616-21104777 | Common:2; Rare:27 | ||||
| chr14:21268903-21268939 | Rare:17 | ||||
| chr14:21269389-21269675 | Common:1; Rare:88 |