| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43120840-43120948 | Common:1; Rare:52 | ||||
| chr5:43121404-43121655 | Common:1; Rare:96 | ||||
| chr5:43192048-43192232 | Common:2; Rare:44 | ||||
| chr5:43313393-43313665 | Common:3; Rare:73 | ||||
| chr5:43483837-43483980 | Common:1; Rare:48 | ||||
| chr5:43515120-43515247 | Common:2; Rare:53 | ||||
| chr5:43602553-43602721 | Common:2; Rare:29 | ||||
| chr5:43603054-43603259 | Rare:52 | ||||
| chr5:44389378-44389641 | Rare:36 | ||||
| chr5:44808721-44808982 | Common:2; Rare:94 | ||||
| chr5:52787823-52787971 | Common:1; Rare:28 | ||||
| chr5:52989171-52989421 | Common:4; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:53109716-53109909 | Common:1; Rare:98; Clinvar:3 | ||||
| chr5:54310513-54310717 | Common:1; Rare:66 | ||||
| chr5:55160090-55160200 | Rare:28 |