| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43557350-43557477 | Rare:29 | ||||
| chr5:43602886-43603285 | Rare:97 | ||||
| chr5:44808722-44809020 | Common:2; Rare:113 | ||||
| chr5:44809377-44809532 | Rare:78 | ||||
| chr5:50441079-50441117 | Rare:18 | ||||
| chr5:50441204-50441457 | Common:3; Rare:73 | ||||
| chr5:50665612-50665922 | Common:1; Rare:39 | ||||
| chr5:50667235-50667570 | Common:1; Rare:108 | ||||
| chr5:50667768-50667957 | Common:1; Rare:59 | ||||
| chr5:51383043-51383092 | Common:1; Rare:19 | ||||
| chr5:51383250-51383405 | Common:1; Rare:55 | ||||
| chr5:52787678-52787950 | Common:1; Rare:56 | ||||
| chr5:52989067-52989365 | Common:5; Rare:84; Clinvar (benign):1 | ||||
| chr5:53109710-53109932 | Common:1; Rare:109; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr5:54310434-54310714 | Common:1; Rare:84 |