| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66345049-66345203 | Common:1; Rare:43 | ||||
| chr11:66480217-66480450 | Common:3; Rare:61 | ||||
| chr11:66593044-66593209 | Common:1; Rare:57 | ||||
| chr11:66616422-66616636 | Common:1; Rare:56 | ||||
| chr11:66677775-66678125 | Common:1; Rare:125 | ||||
| chr11:66744639-66744859 | Common:3; Rare:93 | ||||
| chr11:67353499-67353838 | Common:2; Rare:89 | ||||
| chr11:67401778-67402142 | Common:4; Rare:129 | ||||
| chr11:67428305-67428531 | Rare:78 | ||||
| chr11:67482941-67483154 | Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68030381-68030734 | Common:3; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68213609-68213935 | Common:1; Rare:188 | ||||
| chr11:68271891-68272028 | Common:1; Rare:65 | ||||
| chr11:68460560-68460799 | Common:3; Rare:86 | ||||
| chr11:68903791-68903938 | Common:4; Rare:67; Clinvar (benign):6 |