| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:36874779-36874838 | Rare:30 | ||||
| chr6:36874939-36875168 | Common:1; Rare:35 | ||||
| chr6:36885815-36886011 | Common:3; Rare:67 | ||||
| chr6:37433154-37433309 | Common:2; Rare:43 | ||||
| chr6:39115155-39115234 | Common:1; Rare:18 | ||||
| chr6:41723524-41723696 | Common:2; Rare:46 | ||||
| chr6:41921076-41921192 | Common:1; Rare:29 | ||||
| chr6:42217846-42217987 | Common:3; Rare:36 | ||||
| chr6:42747067-42747193 | Rare:27 | ||||
| chr6:42879576-42879940 | Rare:108 | ||||
| chr6:42929204-42929545 | Common:4; Rare:94 | ||||
| chr6:42984307-42984655 | Rare:99 | ||||
| chr6:43013869-43014269 | Common:2; Rare:87 | ||||
| chr6:43427780-43427915 | Rare:34 | ||||
| chr6:43516876-43517112 | Common:4; Rare:91; Clinvar:2; Clinvar (benign):1 |