| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77141778-77141946 | Common:1; Rare:25 | ||||
| chr14:77377022-77377415 | Common:3; Rare:117 | ||||
| chr14:77457550-77457886 | Common:2; Rare:99 | ||||
| chr14:77457987-77458151 | Rare:47 | ||||
| chr14:77707979-77708131 | Common:1; Rare:80 | ||||
| chr14:77761116-77761203 | Rare:41 | ||||
| chr14:81220699-81221069 | Common:3; Rare:142 | ||||
| chr14:81221279-81221541 | Common:1; Rare:82 | ||||
| chr14:85530004-85530200 | Common:1; Rare:41 | ||||
| chr14:88551451-88551597 | Common:2; Rare:35 | ||||
| chr14:88562952-88563123 | Rare:83 | ||||
| chr14:88824337-88824708 | Common:2; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:89349956-89350317 | Rare:72 | ||||
| chr14:89619091-89619264 | Common:1; Rare:62 | ||||
| chr14:89954656-89954950 | Rare:90 |