| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1633926-1634047 | Common:2; Rare:41 | ||||
| chr5:1931049-1931213 | Common:2; Rare:40 | ||||
| chr5:1931726-1931763 | Rare:10 | ||||
| chr5:2334793-2335066 | Rare:68 | ||||
| chr5:8457537-8457730 | Common:1; Rare:70 | ||||
| chr5:12574547-12574845 | Common:4; Rare:96 | ||||
| chr5:14011736-14011850 | Common:1; Rare:36 | ||||
| chr5:40059417-40059644 | Common:6; Rare:56 | ||||
| chr5:43066122-43066439 | Common:3; Rare:82 | ||||
| chr5:43066950-43067066 | Rare:30 | ||||
| chr5:54648657-54648937 | Common:2; Rare:74 | ||||
| chr5:60416134-60416314 | Common:1; Rare:39 | ||||
| chr5:65925573-65925907 | Rare:134 | ||||
| chr5:71222325-71222414 | |||||
| chr5:77412993-77413173 | Common:1; Rare:38; Clinvar (benign):1 |