| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:40835184-40835423 | Common:2; Rare:96 | ||||
| chr5:41870364-41870553 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:41925144-41925331 | Common:1; Rare:74 | ||||
| chr5:43120840-43120938 | Common:1; Rare:48 | ||||
| chr5:43121369-43121696 | Common:1; Rare:121 | ||||
| chr5:43191992-43192276 | Common:2; Rare:73 | ||||
| chr5:43397083-43397232 | Rare:24 | ||||
| chr5:43483822-43483959 | Common:3; Rare:47 | ||||
| chr5:43484328-43484502 | Rare:39 | ||||
| chr5:43515105-43515220 | Common:2; Rare:45 | ||||
| chr5:43603068-43603256 | Rare:48 | ||||
| chr5:44808715-44808959 | Common:2; Rare:80 | ||||
| chr5:50441185-50441393 | Common:2; Rare:56 | ||||
| chr5:53109716-53109871 | Common:1; Rare:82; Clinvar:3 | ||||
| chr5:54310565-54310714 | Rare:44 |