| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:120306681-120306867 | Common:2; Rare:44 | ||||
| chr11:120335859-120336022 | Common:1; Rare:30 | ||||
| chr11:120432118-120432219 | Rare:18 | ||||
| chr11:120546705-120546823 | Common:1; Rare:22 | ||||
| chr11:120547903-120548038 | Common:1; Rare:21 | ||||
| chr11:120566267-120566460 | Rare:37 | ||||
| chr11:120952929-120953090 | Common:4; Rare:49 | ||||
| chr11:121129820-121130380 | Common:3; Rare:175; Clinvar:11; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
| chr11:121427226-121427372 | Common:1; Rare:54 | ||||
| chr11:121466590-121467010 | Common:1; Rare:75 | ||||
| chr11:121655233-121655451 | Common:2; Rare:36 | ||||
| chr11:121655608-121655757 | Rare:24 | ||||
| chr11:121688970-121689126 | Common:1; Rare:23 | ||||
| chr11:121689280-121689531 | Common:1; Rare:42 | ||||
| chr11:122025917-122026085 | Rare:43 |