| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43067338-43067495 | Rare:22 | ||||
| chr5:43121396-43121648 | Common:1; Rare:96 | ||||
| chr5:43313378-43313657 | Common:3; Rare:75 | ||||
| chr5:43483830-43483955 | Common:1; Rare:45 | ||||
| chr5:43515021-43515190 | Common:3; Rare:48 | ||||
| chr5:43556849-43556951 | Common:3; Rare:39 | ||||
| chr5:43556997-43557198 | Common:1; Rare:54 | ||||
| chr5:43603061-43603277 | Rare:56 | ||||
| chr5:44808711-44809043 | Common:2; Rare:121 | ||||
| chr5:50667232-50667419 | Common:1; Rare:60 | ||||
| chr5:50667767-50667964 | Common:1; Rare:61 | ||||
| chr5:52989188-52989419 | Common:4; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:53109725-53109916 | Common:1; Rare:97; Clinvar:2 | ||||
| chr5:54310513-54310711 | Rare:63 | ||||
| chr5:54985808-54986211 | Common:1; Rare:60 |