| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:70271471-70271664 | Common:1; Rare:32 | ||||
| chr11:70398236-70398690 | Common:4; Rare:156 | ||||
| chr11:71251811-71252081 | Common:2; Rare:54 | ||||
| chr11:71252395-71252656 | Common:2; Rare:68 | ||||
| chr11:71252671-71253377 | Common:5; Rare:152 | ||||
| chr11:71448285-71448691 | Common:4; Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:71452960-71453293 | Common:4; Rare:94 | ||||
| chr11:71453473-71453515 | Common:1; Rare:7 | ||||
| chr11:71453656-71453701 | Rare:7 | ||||
| chr11:71480742-71481012 | Common:3; Rare:80 | ||||
| chr11:71786762-71787092 | Common:2; Rare:97 | ||||
| chr11:71787189-71787305 | Common:2; Rare:37 | ||||
| chr11:71787362-71787743 | Common:16; Rare:174 | ||||
| chr11:71787745-71787795 | Rare:22 | ||||
| chr11:71927937-71928558 | Common:3; Rare:145 |