| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14124748-14125093 | Common:4; Rare:102; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178573-14178857 | Common:2; Rare:147; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:14402437-14402606 | Rare:45 | ||||
| chr3:15427510-15427631 | Rare:38 | ||||
| chr3:15601522-15601746 | Common:4; Rare:91 | ||||
| chr3:16264896-16265220 | Common:2; Rare:98 | ||||
| chr3:19946989-19947131 | Common:2; Rare:47 | ||||
| chr3:23916926-23917173 | Rare:89 | ||||
| chr3:39051955-39052019 | Common:1; Rare:24 | ||||
| chr3:42804443-42804631 | Common:2; Rare:54 | ||||
| chr3:44761600-44761783 | Common:3; Rare:63 | ||||
| chr3:44976126-44976279 | Common:2; Rare:66 | ||||
| chr3:48440087-48440291 | Common:1; Rare:71 | ||||
| chr3:49411894-49412213 | Common:1; Rare:111 | ||||
| chr3:51385006-51385356 | Common:2; Rare:108 |