| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:117200001-117200207 | Common:5; Rare:43 | ||||
| chr11:117202525-117202923 | Common:1; Rare:64 | ||||
| chr11:117232030-117232185 | Rare:41 | ||||
| chr11:117232520-117232725 | Common:2; Rare:70 | ||||
| chr11:117316078-117316408 | Common:1; Rare:86 | ||||
| chr11:117327965-117328191 | Common:1; Rare:49 | ||||
| chr11:117797142-117797311 | Common:1; Rare:69 | ||||
| chr11:117876607-117876816 | Rare:62 | ||||
| chr11:117986254-117986494 | Common:5; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:117986771-117987070 | Common:1; Rare:60 | ||||
| chr11:117987184-117987457 | Rare:59 | ||||
| chr11:117989722-117990053 | Common:1; Rare:48 | ||||
| chr11:118264283-118264586 | Common:1; Rare:50 | ||||
| chr11:118344268-118344407 | Common:1; Rare:24; Clinvar (benign):1 | ||||
| chr11:118359410-118359659 | Common:3; Rare:104 |