| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15427501-15427652 | Rare:52 | ||||
| chr3:15601509-15601746 | Common:4; Rare:96 | ||||
| chr3:16264907-16265243 | Common:2; Rare:104 | ||||
| chr3:17742596-17742845 | Common:3; Rare:86 | ||||
| chr3:20186176-20186359 | Common:1; Rare:53 | ||||
| chr3:23916916-23917208 | Rare:111 | ||||
| chr3:28349007-28349162 | Common:2; Rare:44 | ||||
| chr3:32570766-32570943 | Common:1; Rare:84 | ||||
| chr3:33798567-33798639 | Common:2; Rare:22 | ||||
| chr3:36993165-36993510 | Common:2; Rare:92; Clinvar:16; Clinvar (benign):6 | ||||
| chr3:37243116-37243330 | Common:3; Rare:65 | ||||
| chr3:39051944-39052032 | Common:1; Rare:32 | ||||
| chr3:40309540-40309807 | Common:7; Rare:94 | ||||
| chr3:40457135-40457368 | Common:3; Rare:100 | ||||
| chr3:41962030-41962274 | Common:4; Rare:60 |