| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77707944-77708204 | Common:5; Rare:316 | ||||
| chr14:77760428-77760817 | Common:4; Rare:166 | ||||
| chr14:77761029-77761204 | Rare:138 | ||||
| chr14:77799955-77800550 | Common:8; Rare:234 | ||||
| chr14:79279154-79279643 | Common:7; Rare:206 | ||||
| chr14:80941640-80942018 | Common:8; Rare:163 | ||||
| chr14:81220675-81221615 | Common:10; Rare:782 | ||||
| chr14:81324088-81324370 | Common:2; Rare:65 | ||||
| chr14:81436393-81436662 | Common:10; Rare:260 | ||||
| chr14:81533744-81534201 | Common:2; Rare:204 | ||||
| chr14:87988477-87988877 | Common:9; Rare:151; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr14:87992038-87992960 | Common:7; Rare:421; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:87992965-87993312 | Common:10; Rare:371; Clinvar:36; Clinvar (benign):18; Clinvar (pathogenic):14 | ||||
| chr14:88384886-88385798 | Common:7; Rare:302; Clinvar:3 | ||||
| chr14:88468960-88469495 | Common:3; Rare:149 |