| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35122194-35122302 | Rare:27 | ||||
| chr14:35122465-35122794 | Common:2; Rare:101 | ||||
| chr14:35292179-35292470 | Common:5; Rare:106; Clinvar:1 | ||||
| chr14:35402746-35403259 | Common:5; Rare:166; Clinvar (benign):4 | ||||
| chr14:35403667-35403915 | Common:1; Rare:95; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:35404423-35404915 | Common:3; Rare:156; Clinvar:1; Clinvar (benign):5 | ||||
| chr14:35809041-35809296 | Common:1; Rare:63 | ||||
| chr14:35826702-35826931 | Common:1; Rare:63 | ||||
| chr14:36320538-36320764 | Common:4; Rare:80 | ||||
| chr14:37197802-37198082 | Common:3; Rare:99 | ||||
| chr14:38256061-38256221 | Common:1; Rare:44 | ||||
| chr14:39114123-39114356 | Common:2; Rare:77 | ||||
| chr14:39170203-39170707 | Common:6; Rare:141 | ||||
| chr14:39175000-39175281 | Common:3; Rare:97 | ||||
| chr14:39267035-39267433 | Common:2; Rare:142 |