| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:44389654-44389731 | Common:1; Rare:27 | ||||
| chr5:44808671-44809016 | Common:2; Rare:126 | ||||
| chr5:50667208-50667429 | Common:1; Rare:73 | ||||
| chr5:51383239-51383553 | Common:2; Rare:115 | ||||
| chr5:51383843-51383925 | Rare:18 | ||||
| chr5:52787813-52787950 | Common:1; Rare:24 | ||||
| chr5:52788327-52788509 | Common:1; Rare:50 | ||||
| chr5:53109711-53109921 | Common:1; Rare:106; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr5:54310513-54310712 | Rare:64 | ||||
| chr5:55307589-55308043 | Common:5; Rare:168 | ||||
| chr5:56909448-56909627 | Common:2; Rare:49 | ||||
| chr5:56909800-56910113 | Common:3; Rare:83 | ||||
| chr5:56952095-56952325 | Rare:86 | ||||
| chr5:57173525-57174202 | Common:3; Rare:236 | ||||
| chr5:58460071-58460246 | Common:4; Rare:69 |