| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:88824312-88824731 | Common:2; Rare:122; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:88824835-88824857 | Rare:9 | ||||
| chr14:88840886-88841126 | Common:2; Rare:78; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:89619064-89619260 | Common:1; Rare:71 | ||||
| chr14:89954644-89954970 | Rare:102 | ||||
| chr14:90256481-90256607 | Common:1; Rare:40 | ||||
| chr14:90331900-90332203 | Common:1; Rare:87 | ||||
| chr14:90396887-90397114 | Common:2; Rare:119 | ||||
| chr14:90397117-90397232 | Common:3; Rare:44; Clinvar (benign):2 | ||||
| chr14:91114010-91114159 | Common:1; Rare:50 | ||||
| chr14:91510239-91510383 | Rare:53 | ||||
| chr14:91510457-91510644 | Common:1; Rare:59 | ||||
| chr14:91836428-91836681 | Common:12; Rare:43 | ||||
| chr14:91946995-91947131 | Common:1; Rare:20 | ||||
| chr14:91947186-91947731 | Common:6; Rare:141; Clinvar:3; Clinvar (benign):9 |