| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34439161-34439218 | Common:1; Rare:15 | ||||
| chr11:34915261-34915570 | Common:2; Rare:45 | ||||
| chr11:34915704-34915935 | Common:4; Rare:52 | ||||
| chr11:34915945-34916395 | Common:7; Rare:155; Clinvar:3; Clinvar (benign):6 | ||||
| chr11:34916403-34916737 | Common:10; Rare:135; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:34916819-34916896 | Rare:24; Clinvar (benign):2 | ||||
| chr11:34917016-34917190 | Common:1; Rare:43 | ||||
| chr11:35139040-35139196 | Common:1; Rare:29 | ||||
| chr11:35139634-35139723 | Rare:20 | ||||
| chr11:35617842-35618034 | Rare:37 | ||||
| chr11:35618131-35618275 | Common:4; Rare:31 | ||||
| chr11:35618280-35618642 | Common:1; Rare:119 | ||||
| chr11:35618741-35619011 | Common:1; Rare:91 | ||||
| chr11:35619079-35619933 | Common:3; Rare:287 | ||||
| chr11:35620185-35620236 | Common:1; Rare:9 |