| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43121404-43121648 | Common:1; Rare:94 | ||||
| chr5:43313364-43313683 | Common:3; Rare:84 | ||||
| chr5:43483842-43483947 | Common:1; Rare:39 | ||||
| chr5:43603063-43603260 | Rare:49 | ||||
| chr5:44388395-44388497 | Rare:19; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:44808727-44808965 | Common:2; Rare:78 | ||||
| chr5:50667541-50667570 | Rare:13 | ||||
| chr5:51383242-51383460 | Common:2; Rare:88 | ||||
| chr5:52787823-52787950 | Common:1; Rare:20 | ||||
| chr5:53109716-53109870 | Common:1; Rare:82; Clinvar:3 | ||||
| chr5:54310482-54310711 | Rare:71 | ||||
| chr5:55307639-55308059 | Common:5; Rare:149 | ||||
| chr5:55534949-55535198 | Common:1; Rare:84 | ||||
| chr5:55994815-55995184 | Rare:127 | ||||
| chr5:56909476-56909629 | Common:1; Rare:42 |