| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31207589-31207951 | Common:2; Rare:124 | ||||
| chr14:31208103-31208318 | Common:2; Rare:54 | ||||
| chr14:31419861-31420261 | Common:4; Rare:119 | ||||
| chr14:31420490-31420782 | Common:5; Rare:96 | ||||
| chr14:31457385-31457614 | Common:2; Rare:74 | ||||
| chr14:31561306-31561476 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32075800-32076123 | Common:2; Rare:66 | ||||
| chr14:32076551-32077114 | Common:3; Rare:155 | ||||
| chr14:32078041-32078281 | Common:1; Rare:58 | ||||
| chr14:32329207-32329368 | Rare:25 | ||||
| chr14:32934395-32934709 | Common:7; Rare:94 | ||||
| chr14:32935121-32935333 | Rare:33 | ||||
| chr14:32939500-32939940 | Common:1; Rare:90 | ||||
| chr14:33951064-33951249 | Common:1; Rare:61 | ||||
| chr14:34462196-34462602 | Common:1; Rare:144 |