| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138931467-138931730 | Common:2; Rare:48 | ||||
| chr5:138932348-138932710 | Common:2; Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:139382493-139382750 | Rare:73 | ||||
| chr5:139388335-139388491 | Common:2; Rare:28 | ||||
| chr5:139389875-139390042 | Rare:32 | ||||
| chr5:139404050-139404109 | Rare:33 | ||||
| chr5:139439469-139439615 | Common:2; Rare:37 | ||||
| chr5:139561121-139561439 | Common:1; Rare:130 | ||||
| chr5:139561659-139561800 | Rare:51 | ||||
| chr5:140107615-140107856 | Rare:87 | ||||
| chr5:140108028-140108173 | Rare:44 | ||||
| chr5:140346580-140346678 | Rare:32 | ||||
| chr5:140401393-140401703 | Common:2; Rare:62 | ||||
| chr5:140547424-140547714 | Common:3; Rare:60 | ||||
| chr5:140564273-140564470 | Common:2; Rare:59 |