| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1763692-1764165 | Common:9; Rare:454; Clinvar:28; Clinvar (benign):24 | ||||
| chr11:1830850-1831140 | Common:1; Rare:71 | ||||
| chr11:1833980-1834502 | Common:1; Rare:270 | ||||
| chr11:2168715-2169328 | Common:10; Rare:243 | ||||
| chr11:2270574-2270802 | Common:4; Rare:87 | ||||
| chr11:2270940-2271266 | Common:9; Rare:202 | ||||
| chr11:2400214-2401000 | Common:31; Rare:689 | ||||
| chr11:2401110-2401929 | Common:20; Rare:325 | ||||
| chr11:2444476-2445087 | Common:7; Rare:208; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:2902007-2902412 | Common:4; Rare:171 | ||||
| chr11:2902484-2903020 | Common:6; Rare:145 | ||||
| chr11:2929280-2929840 | Common:3; Rare:348 | ||||
| chr11:2988392-2988819 | Common:5; Rare:216 | ||||
| chr11:2992213-2992651 | Common:7; Rare:404 | ||||
| chr11:3057331-3057573 | Rare:236 |