| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68347590-68348161 | Common:3; Rare:267; Clinvar:9; Clinvar (benign):3 | ||||
| chr11:68386051-68386654 | Common:2; Rare:175; Clinvar:5; Clinvar (pathogenic):4 | ||||
| chr11:68845410-68845770 | Common:3; Rare:130 | ||||
| chr11:69615580-69615870 | Rare:120 | ||||
| chr11:71152551-71153020 | Common:9; Rare:134 | ||||
| chr11:71251840-71252052 | Common:4; Rare:80 | ||||
| chr11:71253126-71253670 | Common:6; Rare:142 | ||||
| chr11:71545040-71545702 | Common:6; Rare:178 | ||||
| chr11:71947400-71947815 | Common:2; Rare:114 | ||||
| chr11:72398050-72398842 | Common:4; Rare:203 | ||||
| chr11:72417550-72418140 | Common:3; Rare:179 | ||||
| chr11:72787460-72787840 | Rare:80 | ||||
| chr11:73158448-73158695 | Common:4; Rare:95 | ||||
| chr11:73176287-73176850 | Common:7; Rare:154 | ||||
| chr11:73309215-73309550 | Common:2; Rare:214 |