| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33015784-33015935 | Common:1; Rare:59 | ||||
| chr11:33039569-33039786 | Common:1; Rare:49 | ||||
| chr11:33161443-33161678 | Common:6; Rare:65 | ||||
| chr11:33257152-33257460 | Common:3; Rare:104 | ||||
| chr11:33736384-33736523 | Common:2; Rare:46 | ||||
| chr11:33774477-33774670 | Common:2; Rare:69 | ||||
| chr11:34052114-34052451 | Common:4; Rare:158 | ||||
| chr11:34105478-34105686 | Common:2; Rare:70 | ||||
| chr11:34916326-34916681 | Common:10; Rare:142; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35139013-35139327 | Common:1; Rare:84 | ||||
| chr11:35525563-35525824 | Rare:67 | ||||
| chr11:36455737-36455781 | Rare:7 | ||||
| chr11:36510236-36510418 | Rare:62 | ||||
| chr11:43358802-43359001 | Rare:96 | ||||
| chr11:44066189-44066339 | Common:1; Rare:37 |