| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120437881-120438191 | Common:2; Rare:118; Clinvar (benign):2 | ||||
| chr12:120446353-120446489 | Common:2; Rare:63 | ||||
| chr12:120469618-120469873 | Common:2; Rare:91 | ||||
| chr12:120495867-120496158 | Common:6; Rare:98 | ||||
| chr12:120581363-120581577 | Common:1; Rare:77 | ||||
| chr12:121399873-121400154 | Common:5; Rare:101 | ||||
| chr12:121802943-121803091 | Rare:34 | ||||
| chr12:122526911-122527281 | Common:3; Rare:119 | ||||
| chr12:122980568-122980816 | Common:1; Rare:87 | ||||
| chr12:123233096-123233486 | Common:2; Rare:126; Clinvar:1 | ||||
| chr12:123584334-123584609 | Common:5; Rare:91 | ||||
| chr12:123601846-123602156 | Common:6; Rare:85 | ||||
| chr12:123633624-123633856 | Common:1; Rare:107; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:130871755-130872122 | Common:4; Rare:147 | ||||
| chr12:131710835-131711110 | Rare:65 |