| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23417501-23417857 | Common:1; Rare:94; Clinvar:11; Clinvar (benign):15; Clinvar (pathogenic):3 | ||||
| chr14:23418209-23418575 | Common:4; Rare:93; Clinvar:19; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
| chr14:23425693-23426085 | Common:1; Rare:96; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):9 | ||||
| chr14:23430558-23430845 | Common:1; Rare:60; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr14:23431416-23431678 | Common:1; Rare:67; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):6 | ||||
| chr14:23432477-23432825 | Rare:83; Clinvar:8; Clinvar (benign):15; Clinvar (pathogenic):4 | ||||
| chr14:31122913-31123138 | Rare:51 | ||||
| chr14:32203267-32203667 | Common:13; Rare:169 | ||||
| chr14:35402008-35402302 | Common:5; Rare:82; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:38254542-38255085 | Common:1; Rare:191 | ||||
| chr14:49633930-49634043 | Common:1; Rare:52; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr14:49862655-49863095 | Common:2; Rare:193 | ||||
| chr14:50792773-50793006 | Rare:55 | ||||
| chr14:52001550-52001857 | Common:1; Rare:66 | ||||
| chr14:61750990-61751207 | Rare:56 |