| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:59642933-59643214 | Common:5; Rare:42 | ||||
| chr5:61360116-61360367 | Common:2; Rare:47 | ||||
| chr5:62354996-62355242 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:65585733-65586012 | Common:2; Rare:59 | ||||
| chr5:65925530-65925809 | Rare:112 | ||||
| chr5:66168928-66168970 | Common:1; Rare:6 | ||||
| chr5:68216477-68216703 | Rare:43 | ||||
| chr5:68251945-68252183 | Common:1; Rare:35 | ||||
| chr5:70112796-70113022 | Common:3; Rare:9 | ||||
| chr5:72108190-72108349 | Rare:37 | ||||
| chr5:72166847-72166995 | Rare:28 | ||||
| chr5:73824928-73825190 | Common:1; Rare:32 | ||||
| chr5:75052546-75052677 | Common:1; Rare:28 | ||||
| chr5:75053773-75053884 | Common:4; Rare:30 | ||||
| chr5:75054014-75054031 | Common:1; Rare:5 |