| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:32829796-32829951 | Common:3; Rare:36 | ||||
| chr11:33774501-33774650 | Common:2; Rare:55 | ||||
| chr11:34105481-34105661 | Common:2; Rare:57 | ||||
| chr11:34916326-34916669 | Common:10; Rare:138; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138971-35139181 | Common:1; Rare:51 | ||||
| chr11:35662623-35662902 | Common:3; Rare:81 | ||||
| chr11:36289393-36289561 | Common:2; Rare:60 | ||||
| chr11:36510236-36510382 | Rare:44 | ||||
| chr11:43358831-43358993 | Rare:82 | ||||
| chr11:45804965-45805180 | Common:3; Rare:51; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:46617246-46617588 | Common:5; Rare:95 | ||||
| chr11:46700553-46700853 | Common:1; Rare:81 | ||||
| chr11:47214840-47214983 | Common:1; Rare:35 | ||||
| chr11:47269948-47270166 | Common:1; Rare:74 | ||||
| chr11:47565500-47565620 | Common:3; Rare:22 |