| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118909118-118909454 | Common:1; Rare:91 | ||||
| chr11:118910413-118910683 | Common:3; Rare:80 | ||||
| chr11:118997980-118998193 | Common:4; Rare:66 | ||||
| chr11:119018280-119018538 | Common:8; Rare:110 | ||||
| chr11:119018624-119018795 | Common:5; Rare:71 | ||||
| chr11:119057120-119057438 | Common:3; Rare:124 | ||||
| chr11:119067736-119067868 | Rare:45 | ||||
| chr11:119206211-119206369 | Common:4; Rare:69; Clinvar:7; Clinvar (benign):4 | ||||
| chr11:119317124-119317297 | Rare:57 | ||||
| chr11:119381597-119381839 | Common:1; Rare:56 | ||||
| chr11:120336160-120336563 | Rare:161 | ||||
| chr11:121292491-121292801 | Rare:93; Clinvar:3 | ||||
| chr11:122882861-122882956 | Rare:26 | ||||
| chr11:123062062-123062283 | Common:5; Rare:98 | ||||
| chr11:123062403-123062672 | Common:4; Rare:124 |