| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17258768-17258975 | Common:2; Rare:36 | ||||
| chr11:17353004-17353113 | Rare:22 | ||||
| chr11:17353122-17353497 | Common:1; Rare:83 | ||||
| chr11:17353643-17353828 | Common:4; Rare:58 | ||||
| chr11:17531955-17532077 | Rare:22 | ||||
| chr11:17541463-17541757 | Common:2; Rare:52 | ||||
| chr11:17542317-17542551 | Common:2; Rare:38 | ||||
| chr11:17543008-17543546 | Common:5; Rare:89 | ||||
| chr11:17560407-17560715 | Common:1; Rare:64; Clinvar (benign):1 | ||||
| chr11:18383673-18383813 | Rare:31 | ||||
| chr11:18384267-18384487 | Common:1; Rare:36 | ||||
| chr11:18589460-18589472 | Rare:1 | ||||
| chr11:18633366-18633498 | Rare:24 | ||||
| chr11:18707012-18707153 | Common:2; Rare:38 | ||||
| chr11:18900529-18900685 | Rare:34 |