| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:71448298-71448794 | Common:5; Rare:127; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71787303-71787546 | Common:15; Rare:91 | ||||
| chr11:71928419-71928715 | Rare:82 | ||||
| chr11:71928889-71929073 | Common:1; Rare:62 | ||||
| chr11:72039802-72039861 | Rare:3 | ||||
| chr11:72040758-72040880 | Rare:23 | ||||
| chr11:72040998-72041295 | Common:1; Rare:59 | ||||
| chr11:72041398-72041614 | Rare:29 | ||||
| chr11:72041811-72041904 | Common:2; Rare:16 | ||||
| chr11:72041913-72042012 | Rare:22 | ||||
| chr11:72080274-72080341 | Common:3; Rare:9 | ||||
| chr11:72080425-72080670 | Common:1; Rare:60; Clinvar:5 | ||||
| chr11:72080685-72080853 | Rare:38; Clinvar:2 | ||||
| chr11:72112223-72112539 | Rare:80 | ||||
| chr11:72112653-72112875 | Common:3; Rare:99 |