| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67435357-67435450 | Common:1; Rare:22 | ||||
| chr11:71745683-71745915 | Common:6; Rare:62 | ||||
| chr11:114058563-114058887 | Common:5; Rare:67 | ||||
| chr11:114158164-114158188 | Rare:3 | ||||
| chr11:114241985-114242258 | Rare:58 | ||||
| chr11:114258362-114258703 | Common:2; Rare:60 | ||||
| chr11:120126932-120127252 | Common:1; Rare:61 | ||||
| chr11:120133680-120133726 | Rare:7 | ||||
| chr11:134276097-134276193 | Common:2; Rare:21 | ||||
| chr12:16762-16850 | Common:5; Rare:31 | ||||
| chr12:754091-754282 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):3 | ||||
| chr12:2797469-2797778 | Common:1; Rare:76 | ||||
| chr12:2799607-2799860 | Rare:46 | ||||
| chr12:6963025-6963240 | Common:1; Rare:39 | ||||
| chr12:8242933-8243250 | Common:8; Rare:89 |