| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:103078501-103078802 | Common:1; Rare:58 | ||||
| chr11:103133482-103133587 | Rare:20; Clinvar:1 | ||||
| chr11:103167017-103167026 | |||||
| chr11:103409055-103409148 | Common:1; Rare:18 | ||||
| chr11:103410487-103410610 | Common:2; Rare:11 | ||||
| chr11:103665061-103665261 | Common:3; Rare:20 | ||||
| chr11:106827960-106828068 | Common:1; Rare:26 | ||||
| chr11:107908754-107908785 | Rare:3 | ||||
| chr11:108112412-108112577 | Rare:33 | ||||
| chr11:108334823-108335041 | Common:1; Rare:45; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:108584148-108584291 | Rare:25 | ||||
| chr11:110081681-110081895 | Rare:37 | ||||
| chr11:110104019-110104178 | Rare:28 | ||||
| chr11:110183043-110183193 | Common:1; Rare:32 | ||||
| chr11:111555237-111555341 | Rare:38 |