| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:77619683-77619885 | Common:1; Rare:37 | ||||
| chr11:77637710-77637887 | Common:1; Rare:57 | ||||
| chr11:77820930-77821224 | Common:1; Rare:87 | ||||
| chr11:77994648-77994992 | Common:1; Rare:100 | ||||
| chr11:78023215-78023296 | Common:1; Rare:33 | ||||
| chr11:78079745-78079942 | Common:2; Rare:61 | ||||
| chr11:78109152-78109473 | Common:2; Rare:69; Clinvar (pathogenic):1 | ||||
| chr11:78139590-78139842 | Common:3; Rare:96; Clinvar:2 | ||||
| chr11:78188592-78188941 | Common:2; Rare:110 | ||||
| chr11:78417742-78418013 | Common:2; Rare:110 | ||||
| chr11:78574784-78574972 | Common:2; Rare:71; Clinvar (benign):1 | ||||
| chr11:82845796-82846116 | Common:1; Rare:58 | ||||
| chr11:82846124-82846255 | Rare:26 | ||||
| chr11:82900390-82900496 | Rare:33 | ||||
| chr11:83071761-83072111 | Common:4; Rare:101 |