| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35403760-35404220 | Common:2; Rare:257; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:35404563-35404845 | Common:4; Rare:179; Clinvar:2; Clinvar (benign):5 | ||||
| chr14:35826115-35826468 | Rare:155 | ||||
| chr14:35826707-35826929 | Common:2; Rare:114 | ||||
| chr14:36320569-36320823 | Common:6; Rare:153 | ||||
| chr14:37171807-37172145 | Rare:81 | ||||
| chr14:37172352-37173020 | Common:9; Rare:288 | ||||
| chr14:37197806-37198111 | Common:6; Rare:177 | ||||
| chr14:37594788-37595972 | Common:10; Rare:513 | ||||
| chr14:37596080-37596350 | Common:1; Rare:123 | ||||
| chr14:39102523-39102764 | Rare:103 | ||||
| chr14:39103029-39103361 | Common:4; Rare:167 | ||||
| chr14:39114137-39114363 | Common:4; Rare:131 | ||||
| chr14:39170239-39170491 | Common:6; Rare:144 | ||||
| chr14:39174894-39175307 | Common:12; Rare:272 |