| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:71448281-71448690 | Common:4; Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:71787349-71787548 | Common:12; Rare:84 | ||||
| chr11:71928929-71929067 | Common:1; Rare:47 | ||||
| chr11:72041015-72041270 | Common:1; Rare:48 | ||||
| chr11:72041534-72041746 | Rare:32 | ||||
| chr11:72041846-72041893 | Common:1; Rare:9 | ||||
| chr11:72080420-72080769 | Common:2; Rare:82; Clinvar:7 | ||||
| chr11:72103206-72103498 | Rare:81 | ||||
| chr11:72112228-72112483 | Rare:60 | ||||
| chr11:72112656-72112811 | Common:1; Rare:69 | ||||
| chr11:73598051-73598271 | Common:3; Rare:57 | ||||
| chr11:73760577-73760739 | Common:2; Rare:39 | ||||
| chr11:73876778-73877036 | Common:5; Rare:73 | ||||
| chr11:74170831-74171396 | Common:3; Rare:180 | ||||
| chr11:74398375-74398556 | Common:3; Rare:42 |