| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44246055-44246318 | Rare:69 | ||||
| chr6:44246904-44247193 | Common:4; Rare:121 | ||||
| chr6:44387445-44387782 | Common:4; Rare:90 | ||||
| chr6:45377860-45378198 | Common:2; Rare:116 | ||||
| chr6:46129766-46130171 | Common:5; Rare:128 | ||||
| chr6:46325626-46325795 | Rare:25 | ||||
| chr6:46491941-46492031 | Rare:16 | ||||
| chr6:46652708-46653018 | Rare:78 | ||||
| chr6:46921817-46922089 | Common:3; Rare:71 | ||||
| chr6:47477670-47478274 | Common:5; Rare:181; Clinvar:7; Clinvar (benign):8 | ||||
| chr6:49463174-49463423 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52284709-52285091 | Common:2; Rare:125 | ||||
| chr6:52420070-52420386 | Common:3; Rare:132; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52671054-52671171 | Rare:32 | ||||
| chr6:52995249-52995819 | Common:4; Rare:232 |