| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69640983-69641363 | Common:1; Rare:93 | ||||
| chr11:69675150-69675545 | Common:2; Rare:130 | ||||
| chr11:70203113-70203358 | Common:4; Rare:95 | ||||
| chr11:70270444-70270835 | Common:2; Rare:150 | ||||
| chr11:70271689-70271946 | Rare:36 | ||||
| chr11:70398262-70398614 | Common:4; Rare:124 | ||||
| chr11:71440942-71441246 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:71448328-71448703 | Common:4; Rare:100; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71787350-71787592 | Common:13; Rare:108 | ||||
| chr11:71928349-71928472 | Rare:33 | ||||
| chr11:71928572-71928688 | Rare:30 | ||||
| chr11:71928915-71929089 | Common:1; Rare:54 | ||||
| chr11:72040998-72041216 | Common:1; Rare:42 | ||||
| chr11:72041230-72041426 | Rare:33 | ||||
| chr11:72041516-72041918 | Common:2; Rare:75 |