| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:79279926-79280083 | Rare:35 | ||||
| chr14:80211468-80211616 | Rare:24 | ||||
| chr14:81220593-81221054 | Common:5; Rare:151 | ||||
| chr14:81221246-81221471 | Common:1; Rare:54 | ||||
| chr14:85530040-85530176 | Common:1; Rare:31 | ||||
| chr14:88608540-88608818 | Common:1; Rare:49 | ||||
| chr14:88792872-88793045 | Rare:59 | ||||
| chr14:88824405-88824737 | Common:1; Rare:95; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:89954488-89954937 | Common:3; Rare:151 | ||||
| chr14:89956459-89956556 | Common:1; Rare:21 | ||||
| chr14:90331910-90332188 | Common:1; Rare:80 | ||||
| chr14:90397054-90397260 | Common:4; Rare:78; Clinvar (benign):2 | ||||
| chr14:91510210-91510713 | Common:1; Rare:177 | ||||
| chr14:91947214-91947640 | Common:4; Rare:96; Clinvar:1; Clinvar (benign):5 | ||||
| chr14:91947651-91948016 | Common:6; Rare:89; Clinvar:1; Clinvar (benign):2 |