| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:186727285-186727437 | Rare:27 | ||||
| chr5:293086-293190 | Rare:27 | ||||
| chr5:473842-474040 | Common:3; Rare:44 | ||||
| chr5:476565-476773 | Common:2; Rare:82; Clinvar:1 | ||||
| chr5:479916-480165 | Common:3; Rare:71 | ||||
| chr5:784691-784893 | Common:5; Rare:65 | ||||
| chr5:1594349-1594649 | Common:4; Rare:128 | ||||
| chr5:1633909-1634056 | Common:2; Rare:49 | ||||
| chr5:8457507-8457751 | Common:2; Rare:91 | ||||
| chr5:10262882-10263238 | Common:4; Rare:99; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:10290724-10291041 | Rare:72 | ||||
| chr5:14144549-14145065 | Common:3; Rare:138 | ||||
| chr5:14166352-14166654 | Common:1; Rare:47 | ||||
| chr5:14209040-14209356 | Common:1; Rare:57 | ||||
| chr5:14213089-14213129 | Common:1; Rare:6 |