| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:102112827-102112861 | Rare:11 | ||||
| chr11:102317238-102317531 | Rare:58 | ||||
| chr11:102346861-102346951 | Rare:19 | ||||
| chr11:102347024-102347476 | Common:10; Rare:122 | ||||
| chr11:102347766-102348002 | Common:1; Rare:57 | ||||
| chr11:102451806-102452067 | Rare:71 | ||||
| chr11:102452100-102452467 | Common:3; Rare:78 | ||||
| chr11:102452566-102452670 | Common:1; Rare:35 | ||||
| chr11:102452680-102453216 | Common:1; Rare:150 | ||||
| chr11:102780539-102780670 | Common:1; Rare:45 | ||||
| chr11:102797810-102798056 | Common:4; Rare:69 | ||||
| chr11:102798071-102798225 | Common:1; Rare:43 | ||||
| chr11:103091381-103091679 | Rare:66 | ||||
| chr11:103092017-103092321 | Common:3; Rare:103 | ||||
| chr11:103109285-103109586 | Common:1; Rare:90; Clinvar:1; Clinvar (benign):1 |