| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3855004-3855193 | Common:1; Rare:52 | ||||
| chr11:3855586-3855677 | Common:2; Rare:19 | ||||
| chr11:4094549-4095026 | Common:2; Rare:122 | ||||
| chr11:4393640-4393837 | Common:2; Rare:48 | ||||
| chr11:4608171-4608416 | Common:1; Rare:68 | ||||
| chr11:5596009-5596167 | Rare:45 | ||||
| chr11:5624925-5625033 | Rare:17 | ||||
| chr11:6259742-6259902 | Common:3; Rare:38 | ||||
| chr11:6319726-6320020 | Common:2; Rare:74 | ||||
| chr11:6320473-6320609 | Common:2; Rare:49 | ||||
| chr11:6390235-6390502 | Common:2; Rare:78 | ||||
| chr11:6419041-6419155 | Common:2; Rare:22 | ||||
| chr11:6481095-6481585 | Common:5; Rare:182 | ||||
| chr11:6497127-6497308 | Rare:27 | ||||
| chr11:6603515-6603877 | Common:4; Rare:105; Clinvar (benign):3 |