| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:120210808-120211032 | Rare:60 | ||||
| chr11:121292561-121292819 | Rare:88; Clinvar:3 | ||||
| chr11:122655435-122655735 | Rare:61 | ||||
| chr11:122882861-122882950 | Rare:25 | ||||
| chr11:123062047-123062339 | Common:5; Rare:131 | ||||
| chr11:123083082-123083317 | Common:1; Rare:53; Clinvar (pathogenic):1 | ||||
| chr11:123454273-123454698 | Common:3; Rare:70 | ||||
| chr11:123741611-123741891 | Common:2; Rare:75 | ||||
| chr11:124673677-124673955 | Common:5; Rare:84 | ||||
| chr11:124800383-124800685 | Common:1; Rare:100 | ||||
| chr11:124953959-124954212 | Common:5; Rare:74 | ||||
| chr11:125111706-125111996 | Common:3; Rare:60 | ||||
| chr11:125592466-125592914 | Common:6; Rare:153 | ||||
| chr11:125625594-125626007 | Common:4; Rare:138 | ||||
| chr11:125887513-125887737 | Common:2; Rare:66 |