| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15859719-15860153 | Common:9; Rare:252 | ||||
| chr3:16264853-16265256 | Common:4; Rare:269 | ||||
| chr3:17741818-17742340 | Common:2; Rare:261 | ||||
| chr3:17742498-17743022 | Common:9; Rare:333 | ||||
| chr3:19946940-19947412 | Common:11; Rare:334 | ||||
| chr3:20186137-20186415 | Common:6; Rare:153 | ||||
| chr3:23805604-23806071 | Common:4; Rare:125 | ||||
| chr3:23916853-23917224 | Rare:256 | ||||
| chr3:23945121-23945352 | Common:10; Rare:161 | ||||
| chr3:23945810-23946220 | Common:2; Rare:197 | ||||
| chr3:24494738-24494959 | Rare:92 | ||||
| chr3:25428106-25428299 | Rare:70 | ||||
| chr3:25664840-25665086 | Common:5; Rare:131 | ||||
| chr3:25783388-25783669 | Common:4; Rare:167; Clinvar (benign):6 | ||||
| chr3:25789923-25790146 | Common:10; Rare:162 |