| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1350142-1350465 | Common:2; Rare:67 | ||||
| chr11:1517957-1518132 | Rare:32 | ||||
| chr11:1663989-1664140 | Rare:8 | ||||
| chr11:2138323-2138473 | Common:1; Rare:43 | ||||
| chr11:2377998-2378146 | Common:3; Rare:41 | ||||
| chr11:2424128-2424280 | Rare:23 | ||||
| chr11:2695478-2695502 | Rare:3 | ||||
| chr11:2699987-2700279 | Common:2; Rare:115 | ||||
| chr11:2919101-2919264 | Common:2; Rare:40 | ||||
| chr11:4069721-4070085 | Rare:68 | ||||
| chr11:4091122-4091409 | Common:2; Rare:100; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:4666485-4666632 | Common:1; Rare:18 | ||||
| chr11:5293674-5293739 | Common:1; Rare:15 | ||||
| chr11:5518474-5518619 | Common:2; Rare:19 | ||||
| chr11:5683597-5683867 | Common:1; Rare:66 |