| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18105920-18106307 | Common:4; Rare:130 | ||||
| chr11:18322119-18322727 | Common:8; Rare:210; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18341310-18341556 | Rare:73 | ||||
| chr11:18394397-18394634 | Common:1; Rare:94; Clinvar (benign):1 | ||||
| chr11:18526788-18526977 | Common:1; Rare:82 | ||||
| chr11:18588628-18588821 | Common:1; Rare:75 | ||||
| chr11:18634213-18634264 | Rare:11 | ||||
| chr11:18634278-18634592 | Common:3; Rare:111 | ||||
| chr11:18634761-18634865 | Rare:27 | ||||
| chr11:19714057-19714195 | Rare:29 | ||||
| chr11:20364118-20364189 | Rare:16 | ||||
| chr11:20387266-20387665 | Common:9; Rare:121 | ||||
| chr11:22625780-22625918 | Common:2; Rare:57; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:26994027-26994172 | Common:1; Rare:21 | ||||
| chr11:27362838-27362867 | Rare:10 |