| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3157534-3157633 | Common:6; Rare:42 | ||||
| chr6:3324130-3324398 | Rare:57 | ||||
| chr6:3456038-3456175 | Rare:44 | ||||
| chr6:3751341-3751513 | Rare:69 | ||||
| chr6:3849211-3849448 | Common:3; Rare:69 | ||||
| chr6:4021165-4021428 | Rare:113 | ||||
| chr6:5003613-5003843 | Common:6; Rare:72 | ||||
| chr6:5004007-5004084 | Rare:39 | ||||
| chr6:5132780-5133088 | Common:2; Rare:61 | ||||
| chr6:5260671-5261025 | Common:3; Rare:122; Clinvar (benign):4 | ||||
| chr6:7107525-7107838 | Rare:103 | ||||
| chr6:7108603-7108683 | Rare:26 | ||||
| chr6:7313043-7313379 | Common:5; Rare:125 | ||||
| chr6:7389740-7389976 | Common:1; Rare:61 | ||||
| chr6:7910633-7910927 | Common:3; Rare:115 |