| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:72814291-72814448 | Common:2; Rare:51 | ||||
| chr11:73598035-73598281 | Common:3; Rare:62 | ||||
| chr11:73876799-73877019 | Common:4; Rare:55 | ||||
| chr11:74170861-74171472 | Common:3; Rare:193 | ||||
| chr11:74398382-74398538 | Common:3; Rare:29 | ||||
| chr11:74949062-74949307 | Common:6; Rare:69 | ||||
| chr11:75562105-75562303 | Common:1; Rare:52; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:76444665-76444900 | Rare:53 | ||||
| chr11:76444961-76445064 | Common:1; Rare:26 | ||||
| chr11:76783060-76783357 | Common:9; Rare:96 | ||||
| chr11:76860669-76860946 | Common:4; Rare:88 | ||||
| chr11:77637733-77637877 | Common:1; Rare:51 | ||||
| chr11:77820945-77821164 | Common:1; Rare:64 | ||||
| chr11:78079761-78079942 | Common:2; Rare:56 | ||||
| chr11:78139581-78139809 | Common:3; Rare:91; Clinvar:2 |