| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138933617-138933960 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:140243191-140243365 | Rare:47 | ||||
| chr5:140711130-140711275 | Common:1; Rare:38 | ||||
| chr5:148826386-148826632 | Common:3; Rare:63 | ||||
| chr5:149409149-149409851 | Common:3; Rare:124 | ||||
| chr5:149409866-149410191 | Common:2; Rare:55 | ||||
| chr5:149410789-149411139 | Common:3; Rare:80 | ||||
| chr5:149412126-149412323 | Common:3; Rare:39 | ||||
| chr5:149412391-149413036 | Common:8; Rare:144 | ||||
| chr5:149413153-149413623 | Common:4; Rare:94 | ||||
| chr5:149414459-149414931 | Common:4; Rare:76 | ||||
| chr5:149415041-149415131 | Common:3; Rare:15 | ||||
| chr5:149418903-149419214 | Common:3; Rare:40 | ||||
| chr5:149420656-149420829 | Common:1; Rare:44 | ||||
| chr5:149421419-149421764 | Common:5; Rare:64 |