| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:58582019-58582214 | Common:1; Rare:35 | ||||
| chr5:58582897-58583211 | Common:2; Rare:82 | ||||
| chr5:59039835-59039952 | Rare:27 | ||||
| chr5:59356947-59356999 | Rare:8 | ||||
| chr5:60699746-60699822 | Rare:10 | ||||
| chr5:60700060-60700285 | Common:4; Rare:91 | ||||
| chr5:60844175-60844437 | Common:5; Rare:88 | ||||
| chr5:60944992-60945387 | Common:6; Rare:160; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr5:61162215-61162726 | Common:1; Rare:115 | ||||
| chr5:61331549-61331822 | Common:3; Rare:119 | ||||
| chr5:62403746-62404033 | Common:3; Rare:108 | ||||
| chr5:62412512-62412857 | Common:1; Rare:117 | ||||
| chr5:64690127-64690537 | Common:1; Rare:86 | ||||
| chr5:64768509-64769082 | Common:5; Rare:147 | ||||
| chr5:65481906-65481992 | Common:1; Rare:15 |