| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:117144150-117144352 | Common:2; Rare:98 | ||||
| chr11:119018309-119018457 | Common:5; Rare:54 | ||||
| chr11:119018626-119018792 | Common:5; Rare:71 | ||||
| chr11:119067636-119067816 | Common:3; Rare:60 | ||||
| chr11:123062449-123062639 | Common:2; Rare:77 | ||||
| chr11:124673716-124673929 | Common:4; Rare:64 | ||||
| chr11:126211651-126211804 | Rare:70 | ||||
| chr11:126268829-126269154 | Common:1; Rare:116; Clinvar:1 | ||||
| chr11:134253306-134253569 | Common:2; Rare:83; Clinvar (benign):1 | ||||
| chr12:2877022-2877262 | Rare:71 | ||||
| chr12:4538724-4538896 | Common:1; Rare:36 | ||||
| chr12:4648944-4649140 | Common:2; Rare:58; Clinvar (benign):1 | ||||
| chr12:6493230-6493502 | Common:7; Rare:81 | ||||
| chr12:6493770-6494133 | Common:2; Rare:109 | ||||
| chr12:6568255-6568382 | Rare:48 |