| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:50441201-50441427 | Common:2; Rare:64 | ||||
| chr5:50666514-50666737 | Common:3; Rare:60 | ||||
| chr5:50666887-50666972 | Common:1; Rare:26 | ||||
| chr5:50667334-50667410 | Common:1; Rare:24 | ||||
| chr5:50667522-50667570 | Rare:17 | ||||
| chr5:50667768-50667857 | Common:1; Rare:27 | ||||
| chr5:52787851-52787950 | Rare:14 | ||||
| chr5:52989227-52989495 | Common:4; Rare:84; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:53109711-53109890 | Common:1; Rare:91; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr5:54310426-54310711 | Common:1; Rare:84 | ||||
| chr5:55024075-55024256 | Common:2; Rare:29 | ||||
| chr5:55233606-55233882 | Common:4; Rare:99 | ||||
| chr5:55307614-55308146 | Common:5; Rare:196 | ||||
| chr5:55994797-55995199 | Rare:139 | ||||
| chr5:57173537-57173871 | Common:3; Rare:121 |