| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44126687-44126919 | Rare:57 | ||||
| chr6:44127339-44127751 | Common:4; Rare:109 | ||||
| chr6:44219518-44219680 | Common:2; Rare:45 | ||||
| chr6:44246980-44247359 | Common:2; Rare:164 | ||||
| chr6:44256966-44257105 | Common:2; Rare:31 | ||||
| chr6:44257259-44257391 | Rare:39 | ||||
| chr6:44265525-44265710 | Common:1; Rare:93 | ||||
| chr6:44387440-44387858 | Common:4; Rare:113 | ||||
| chr6:44387863-44388141 | Common:5; Rare:80 | ||||
| chr6:45377580-45377741 | Common:2; Rare:61 | ||||
| chr6:45377790-45378189 | Common:2; Rare:129 | ||||
| chr6:46129804-46130136 | Common:5; Rare:109 | ||||
| chr6:46652707-46653031 | Rare:79 | ||||
| chr6:46735267-46735560 | Common:2; Rare:85 | ||||
| chr6:47477514-47478035 | Common:2; Rare:140; Clinvar:3; Clinvar (benign):3 |