| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:41927155-41927751 | Common:4; Rare:212 | ||||
| chr6:41941733-41941977 | Common:2; Rare:128 | ||||
| chr6:42048620-42048783 | Common:3; Rare:127 | ||||
| chr6:42050480-42050970 | Common:3; Rare:194 | ||||
| chr6:42142410-42142980 | Common:8; Rare:261 | ||||
| chr6:42563955-42564343 | Rare:154 | ||||
| chr6:42746059-42746370 | Rare:173 | ||||
| chr6:42746818-42747020 | Rare:80 | ||||
| chr6:42781930-42782734 | Common:4; Rare:158 | ||||
| chr6:42879546-42879999 | Common:1; Rare:292 | ||||
| chr6:42890786-42890979 | Rare:129 | ||||
| chr6:42928900-42929170 | Rare:123 | ||||
| chr6:42929199-42929592 | Common:8; Rare:229 | ||||
| chr6:42960614-42960758 | Common:2; Rare:62 | ||||
| chr6:42978390-42978740 | Rare:111; Clinvar:14; Clinvar (benign):1; Clinvar (pathogenic):3 |