| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:81427406-81427601 | Common:2; Rare:52 | ||||
| chr14:81436413-81436653 | Common:3; Rare:91 | ||||
| chr14:81533745-81534185 | Common:1; Rare:126 | ||||
| chr14:85529810-85529916 | Rare:19 | ||||
| chr14:85529923-85530239 | Common:2; Rare:65 | ||||
| chr14:87992819-87992895 | Rare:19 | ||||
| chr14:87992967-87993085 | Rare:58; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):6 | ||||
| chr14:87993087-87993301 | Common:4; Rare:94; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr14:88385519-88385802 | Common:1; Rare:98; Clinvar:3 | ||||
| chr14:88551419-88551695 | Common:3; Rare:65 | ||||
| chr14:88554666-88554920 | Common:4; Rare:64 | ||||
| chr14:88554945-88555103 | Common:2; Rare:53 | ||||
| chr14:88562853-88563163 | Rare:133 | ||||
| chr14:88563358-88563601 | Rare:91 | ||||
| chr14:88792822-88793091 | Rare:84 |