| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:102317320-102317532 | Rare:50 | ||||
| chr11:102317544-102317669 | Common:2; Rare:37 | ||||
| chr11:102346752-102346840 | Common:1; Rare:18 | ||||
| chr11:102347026-102347542 | Common:11; Rare:142 | ||||
| chr11:102347544-102347609 | Rare:22 | ||||
| chr11:102347612-102347763 | Common:1; Rare:28 | ||||
| chr11:102347795-102347997 | Common:1; Rare:45 | ||||
| chr11:102451752-102452004 | Rare:63 | ||||
| chr11:102452096-102452470 | Common:3; Rare:78 | ||||
| chr11:102452584-102453205 | Common:2; Rare:179 | ||||
| chr11:102798148-102798350 | Common:1; Rare:47 | ||||
| chr11:103091473-103091657 | Rare:44 | ||||
| chr11:103092020-103092331 | Common:3; Rare:107 | ||||
| chr11:103109279-103109527 | Common:1; Rare:65; Clinvar (benign):1 | ||||
| chr11:103109610-103109782 | Common:1; Rare:42; Clinvar:2; Clinvar (pathogenic):1 |