| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:72996643-72996823 | Common:3; Rare:75 | ||||
| chr3:79018999-79019106 | Rare:31 | ||||
| chr3:81761515-81761779 | Common:8; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:87227231-87227349 | Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:88058932-88059308 | Common:3; Rare:140 | ||||
| chr3:88149605-88150043 | Common:6; Rare:132 | ||||
| chr3:94062930-94063069 | Rare:35 | ||||
| chr3:97764491-97764802 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821846-97822084 | Rare:87 | ||||
| chr3:97972390-97972511 | Common:3; Rare:46 | ||||
| chr3:98732385-98732508 | Rare:23 | ||||
| chr3:99817562-99817930 | Rare:109 | ||||
| chr3:99876161-99876278 | Common:1; Rare:29 | ||||
| chr3:100260724-100261057 | Rare:96 | ||||
| chr3:100401402-100401580 | Common:1; Rare:33 |