| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118791261-118791308 | Rare:32 | ||||
| chr11:118997980-118998212 | Common:4; Rare:70 | ||||
| chr11:119018280-119018457 | Common:6; Rare:72 | ||||
| chr11:119018626-119018795 | Common:5; Rare:71 | ||||
| chr11:119057098-119057446 | Common:3; Rare:139 | ||||
| chr11:119067624-119067837 | Common:3; Rare:70 | ||||
| chr11:119095419-119095519 | Common:1; Rare:57 | ||||
| chr11:119121267-119121635 | Common:1; Rare:90 | ||||
| chr11:119206211-119206373 | Common:4; Rare:71; Clinvar:7; Clinvar (benign):4 | ||||
| chr11:119317082-119317275 | Rare:63 | ||||
| chr11:119423135-119423368 | Common:3; Rare:65 | ||||
| chr11:120336221-120336528 | Rare:128 | ||||
| chr11:121292614-121292793 | Rare:58; Clinvar:3 | ||||
| chr11:123062064-123062672 | Common:9; Rare:273 | ||||
| chr11:124673715-124673940 | Common:4; Rare:66 |