| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:45377855-45378220 | Common:2; Rare:122 | ||||
| chr6:46015578-46015921 | Common:2; Rare:74 | ||||
| chr6:46129789-46130180 | Common:5; Rare:124 | ||||
| chr6:46325645-46325819 | Rare:22 | ||||
| chr6:46652688-46653013 | Rare:81 | ||||
| chr6:46735327-46735480 | Common:1; Rare:42 | ||||
| chr6:46921789-46922093 | Common:3; Rare:77 | ||||
| chr6:47477685-47478247 | Common:5; Rare:166; Clinvar:7; Clinvar (benign):7 | ||||
| chr6:49463174-49463412 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:49550457-49550731 | Rare:61 | ||||
| chr6:52284713-52285041 | Common:2; Rare:111 | ||||
| chr6:52420089-52420375 | Common:3; Rare:122; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52576943-52577314 | Common:7; Rare:127 | ||||
| chr6:52995259-52995832 | Common:4; Rare:231 | ||||
| chr6:53065278-53065608 | Common:1; Rare:115 |