| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:71448342-71448644 | Common:3; Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71452963-71453258 | Common:4; Rare:81 | ||||
| chr11:71480128-71480148 | Rare:4 | ||||
| chr11:71928429-71928703 | Rare:73 | ||||
| chr11:72041843-72042030 | Common:2; Rare:36 | ||||
| chr11:72080461-72080835 | Common:2; Rare:84; Clinvar:7 | ||||
| chr11:72112337-72112494 | Rare:42 | ||||
| chr11:72224135-72224197 | Common:3; Rare:12 | ||||
| chr11:72752382-72752516 | Common:2; Rare:39 | ||||
| chr11:72793608-72793767 | Rare:38 | ||||
| chr11:72814304-72814442 | Common:2; Rare:45 | ||||
| chr11:73760570-73760631 | Rare:12 | ||||
| chr11:73787852-73787986 | Common:1; Rare:41 | ||||
| chr11:73876778-73877019 | Common:5; Rare:63 | ||||
| chr11:73983198-73983517 | Common:4; Rare:79 |