| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:28108115-28108414 | Common:1; Rare:90 | ||||
| chr11:30322978-30323195 | Common:2; Rare:62 | ||||
| chr11:31509575-31509796 | Common:1; Rare:71 | ||||
| chr11:32583638-32583929 | Rare:102 | ||||
| chr11:33161449-33161678 | Common:6; Rare:63 | ||||
| chr11:33257157-33257427 | Common:3; Rare:92 | ||||
| chr11:33736391-33736608 | Common:2; Rare:67 | ||||
| chr11:33774493-33774656 | Common:2; Rare:56 | ||||
| chr11:34052126-34052417 | Common:4; Rare:134 | ||||
| chr11:34438784-34439016 | Common:2; Rare:80; Clinvar (benign):1 | ||||
| chr11:34620872-34621150 | Common:2; Rare:59 | ||||
| chr11:34624152-34624302 | Common:2; Rare:34 | ||||
| chr11:34916292-34916658 | Common:10; Rare:148; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138903-35139343 | Common:1; Rare:115 | ||||
| chr11:35662804-35662902 | Rare:30 |