| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50532473-50532733 | Common:2; Rare:79 | ||||
| chr14:50668295-50668560 | Common:4; Rare:98 | ||||
| chr14:50944391-50944636 | Common:4; Rare:84; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51651619-51652159 | Common:6; Rare:149 | ||||
| chr14:52068990-52069215 | Common:2; Rare:53 | ||||
| chr14:52707033-52707240 | Common:1; Rare:91 | ||||
| chr14:52791427-52791757 | Common:1; Rare:111 | ||||
| chr14:52951041-52951395 | Common:4; Rare:127 | ||||
| chr14:53152374-53152437 | Rare:23 | ||||
| chr14:53953363-53953669 | Common:2; Rare:84 | ||||
| chr14:53954467-53954566 | Rare:13 | ||||
| chr14:54566990-54567168 | Rare:46 | ||||
| chr14:55027048-55027309 | Common:2; Rare:72 | ||||
| chr14:55051402-55051775 | Common:1; Rare:157 | ||||
| chr14:55191511-55191756 | Common:5; Rare:56 |