| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:114185494-114185655 | Common:3; Rare:33 | ||||
| chr11:114195686-114195745 | Common:1; Rare:10 | ||||
| chr11:114197828-114198042 | Common:2; Rare:27 | ||||
| chr11:114233677-114233786 | Rare:15 | ||||
| chr11:114245382-114245724 | Common:3; Rare:66 | ||||
| chr11:117838122-117838421 | Common:2; Rare:76 | ||||
| chr11:119312104-119312359 | Common:1; Rare:94 | ||||
| chr11:123074839-123075136 | Common:2; Rare:62 | ||||
| chr11:126266915-126267203 | Common:1; Rare:92 | ||||
| chr11:134148971-134149175 | Common:4; Rare:85 | ||||
| chr12:16769-16847 | Common:4; Rare:28 | ||||
| chr12:753851-754088 | Common:1; Rare:98; Clinvar:6; Clinvar (benign):3 | ||||
| chr12:2797443-2797769 | Common:1; Rare:77 | ||||
| chr12:2843050-2843260 | Common:1; Rare:44 | ||||
| chr12:4275455-4275511 | Common:1; Rare:5 |