| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42929211-42929588 | Common:3; Rare:112 | ||||
| chr6:42984290-42984629 | Rare:83 | ||||
| chr6:43013809-43014329 | Common:2; Rare:130 | ||||
| chr6:43040627-43040962 | Rare:99; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:43516846-43517109 | Common:5; Rare:97; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575962-43576228 | Common:1; Rare:110; Clinvar:8 | ||||
| chr6:43687757-43687921 | Common:2; Rare:59 | ||||
| chr6:43770053-43770509 | Common:7; Rare:114 | ||||
| chr6:44127278-44127639 | Common:4; Rare:97 | ||||
| chr6:44219496-44219651 | Common:1; Rare:39 | ||||
| chr6:44387407-44387753 | Common:4; Rare:87 | ||||
| chr6:45377866-45378092 | Common:2; Rare:80 | ||||
| chr6:46652718-46653013 | Rare:74 | ||||
| chr6:47042315-47042439 | Common:1; Rare:27 | ||||
| chr6:49463174-49463449 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):1 |