| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119206180-119206325 | Common:5; Rare:67; Clinvar:6; Clinvar (benign):4 | ||||
| chr11:119334329-119334529 | Rare:54 | ||||
| chr11:119423127-119423368 | Common:3; Rare:66 | ||||
| chr11:120325207-120325314 | Common:1; Rare:29 | ||||
| chr11:121023985-121024153 | Common:1; Rare:52 | ||||
| chr11:121292569-121292825 | Rare:88; Clinvar:3 | ||||
| chr11:122655569-122655749 | Rare:47 | ||||
| chr11:123062393-123062679 | Common:4; Rare:132 | ||||
| chr11:123654535-123654708 | Common:2; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:123741587-123741756 | Common:1; Rare:44 | ||||
| chr11:124673715-124673823 | Rare:43 | ||||
| chr11:124673826-124673929 | Common:4; Rare:22 | ||||
| chr11:124762240-124762405 | Rare:45 | ||||
| chr11:124800406-124800485 | Rare:31 | ||||
| chr11:124953962-124954213 | Common:5; Rare:73 |