| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:117093716-117093897 | Common:2; Rare:34 | ||||
| chr11:117147324-117147580 | Common:1; Rare:49 | ||||
| chr11:117183809-117184115 | Common:1; Rare:80 | ||||
| chr11:117212126-117212374 | Common:3; Rare:50 | ||||
| chr11:117216949-117216982 | Rare:5 | ||||
| chr11:117272633-117272835 | Rare:24 | ||||
| chr11:117293084-117293299 | Common:1; Rare:58 | ||||
| chr11:117351953-117352043 | Rare:35; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:118244404-118244610 | Common:2; Rare:36 | ||||
| chr11:118266023-118266295 | Common:3; Rare:47 | ||||
| chr11:118439190-118439322 | Rare:22 | ||||
| chr11:118440804-118440988 | Common:1; Rare:29 | ||||
| chr11:118756243-118756282 | Rare:7 | ||||
| chr11:118768266-118768506 | Common:1; Rare:48 | ||||
| chr11:118791671-118791769 | Common:1; Rare:26 |