| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:16175278-16175351 | Rare:14 | ||||
| chr3:16264862-16265233 | Common:2; Rare:125 | ||||
| chr3:17742596-17742952 | Common:4; Rare:124 | ||||
| chr3:18424221-18424568 | Common:6; Rare:72 | ||||
| chr3:19946974-19947245 | Common:4; Rare:97 | ||||
| chr3:19947316-19947415 | Rare:37 | ||||
| chr3:20186169-20186365 | Common:1; Rare:55 | ||||
| chr3:23916876-23917173 | Rare:113 | ||||
| chr3:23917666-23917980 | Common:2; Rare:84; Clinvar (benign):1 | ||||
| chr3:25428107-25428346 | Rare:52 | ||||
| chr3:25789957-25790090 | Common:2; Rare:50 | ||||
| chr3:28348773-28349191 | Common:4; Rare:132 | ||||
| chr3:29280852-29281076 | Common:3; Rare:42 | ||||
| chr3:31981633-31981788 | Common:1; Rare:41 | ||||
| chr3:32570636-32570892 | Rare:117 |