| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67469201-67469407 | Common:3; Rare:68 | ||||
| chr11:67482913-67483171 | Rare:57; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67583648-67583840 | Common:1; Rare:62 | ||||
| chr11:67650193-67650351 | Common:2; Rare:36 | ||||
| chr11:68030412-68030733 | Common:3; Rare:86; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68271917-68272129 | Common:2; Rare:93 | ||||
| chr11:68903784-68903931 | Common:4; Rare:70; Clinvar (benign):6 | ||||
| chr11:69048703-69048988 | Common:6; Rare:105 | ||||
| chr11:69675301-69675493 | Rare:54 | ||||
| chr11:70398358-70398608 | Common:2; Rare:90 | ||||
| chr11:71448352-71448673 | Common:3; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:71452987-71453249 | Common:3; Rare:72 | ||||
| chr11:71928889-71929056 | Common:1; Rare:58 | ||||
| chr11:72080502-72080634 | Rare:26; Clinvar:1 | ||||
| chr11:72103203-72103621 | Rare:109 |