| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1834760-1834784 | Rare:5 | ||||
| chr11:1835307-1835432 | Common:3; Rare:56 | ||||
| chr11:1836517-1836591 | Common:2; Rare:23 | ||||
| chr11:1863185-1863336 | Rare:40 | ||||
| chr11:1863599-1863796 | Common:1; Rare:50 | ||||
| chr11:1876529-1876779 | Common:3; Rare:55 | ||||
| chr11:1947223-1947344 | Common:3; Rare:16 | ||||
| chr11:2400161-2400874 | Common:12; Rare:216 | ||||
| chr11:2401285-2401688 | Common:10; Rare:81 | ||||
| chr11:2884556-2884739 | Common:1; Rare:59; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:2884979-2885251 | Common:1; Rare:78; Clinvar:23; Clinvar (benign):12 | ||||
| chr11:2885723-2885944 | Rare:70; Clinvar:1 | ||||
| chr11:2899480-2899594 | Common:1; Rare:32 | ||||
| chr11:2902004-2902385 | Common:1; Rare:84 | ||||
| chr11:2902588-2902726 | Common:1; Rare:31 |