| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119468844-119469010 | Rare:61 | ||||
| chr3:119498734-119498926 | Rare:67 | ||||
| chr3:119579678-119579796 | Common:3; Rare:26 | ||||
| chr3:119677219-119677475 | Common:1; Rare:96 | ||||
| chr3:120094424-120094771 | Common:4; Rare:109 | ||||
| chr3:120742503-120742777 | Common:2; Rare:77 | ||||
| chr3:121592993-121593093 | Rare:16 | ||||
| chr3:121593280-121593414 | Rare:22 | ||||
| chr3:121749067-121749324 | Rare:40 | ||||
| chr3:121834956-121835248 | Common:3; Rare:99; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383190-122383326 | Common:1; Rare:43 | ||||
| chr3:122384076-122384281 | Common:3; Rare:75 | ||||
| chr3:122416031-122416218 | Common:1; Rare:63 | ||||
| chr3:122564236-122564437 | Common:3; Rare:59 | ||||
| chr3:122794653-122794826 | Rare:28 |