| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43771906-43771985 | Rare:17 | ||||
| chr6:44127351-44127652 | Common:4; Rare:88 | ||||
| chr6:44219496-44219651 | Common:1; Rare:39 | ||||
| chr6:44246914-44247193 | Common:4; Rare:118 | ||||
| chr6:44387445-44387777 | Common:4; Rare:88 | ||||
| chr6:45377614-45377693 | Common:2; Rare:33 | ||||
| chr6:45377790-45378142 | Common:2; Rare:111 | ||||
| chr6:46129774-46129993 | Common:3; Rare:56 | ||||
| chr6:46491895-46492040 | Rare:29 | ||||
| chr6:46652748-46653022 | Rare:70 | ||||
| chr6:46921918-46922080 | Rare:40 | ||||
| chr6:47477602-47478253 | Common:5; Rare:188; Clinvar:7; Clinvar (benign):7 | ||||
| chr6:49463174-49463401 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52995267-52995823 | Common:4; Rare:229 | ||||
| chr6:53065381-53065672 | Common:1; Rare:81 |