| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119559590-119559764 | Common:3; Rare:27 | ||||
| chr3:119677374-119677696 | Rare:83 | ||||
| chr3:119843140-119843281 | Rare:32 | ||||
| chr3:120093694-120093763 | Rare:22 | ||||
| chr3:120596076-120596354 | Common:3; Rare:90 | ||||
| chr3:120742483-120742783 | Common:2; Rare:89 | ||||
| chr3:121643986-121644047 | Rare:11 | ||||
| chr3:121660844-121661004 | Rare:28 | ||||
| chr3:121749647-121750025 | Common:1; Rare:87 | ||||
| chr3:121834975-121835278 | Common:3; Rare:101; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122416027-122416227 | Common:1; Rare:67 | ||||
| chr3:122564227-122564427 | Common:3; Rare:58 | ||||
| chr3:122564568-122564601 | Rare:9 | ||||
| chr3:122577576-122577679 | Rare:26 | ||||
| chr3:122681188-122681281 | Rare:21 |