| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:73597977-73598315 | Common:3; Rare:87 | ||||
| chr11:73760074-73760313 | Rare:56 | ||||
| chr11:73760573-73760818 | Common:2; Rare:58 | ||||
| chr11:73760994-73761331 | Common:3; Rare:104 | ||||
| chr11:73787804-73787942 | Common:1; Rare:33 | ||||
| chr11:73788050-73788156 | Common:2; Rare:21 | ||||
| chr11:73876618-73877060 | Common:5; Rare:133 | ||||
| chr11:73982755-73982962 | Common:7; Rare:77 | ||||
| chr11:74170831-74171385 | Common:3; Rare:177 | ||||
| chr11:74398373-74398538 | Common:3; Rare:34 | ||||
| chr11:74492941-74493406 | Common:2; Rare:144; Clinvar (pathogenic):1 | ||||
| chr11:74493679-74493935 | Common:1; Rare:93 | ||||
| chr11:74592473-74592675 | Common:1; Rare:64 | ||||
| chr11:74748619-74748878 | Common:3; Rare:59 | ||||
| chr11:74949046-74949382 | Common:6; Rare:105 |