| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:10307726-10308067 | Common:2; Rare:122 | ||||
| chr5:10353497-10353994 | Common:8; Rare:348 | ||||
| chr5:10354020-10354340 | Rare:202 | ||||
| chr5:10563710-10564094 | Common:3; Rare:107 | ||||
| chr5:10564153-10564384 | Common:2; Rare:134 | ||||
| chr5:10761083-10761450 | Common:21; Rare:225 | ||||
| chr5:14142975-14143395 | Rare:188 | ||||
| chr5:14581643-14581851 | Rare:86 | ||||
| chr5:14664467-14664962 | Common:7; Rare:280 | ||||
| chr5:14871595-14872048 | Common:6; Rare:232; Clinvar (benign):2 | ||||
| chr5:16465666-16465953 | Common:2; Rare:126 | ||||
| chr5:16508790-16509330 | Common:7; Rare:130 | ||||
| chr5:16936203-16936478 | Common:6; Rare:158 | ||||
| chr5:17216080-17216407 | Rare:94 | ||||
| chr5:17216600-17216952 | Common:1; Rare:102 |