| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:98805312-98805488 | Rare:28 | ||||
| chr3:98806531-98806843 | Common:2; Rare:52 | ||||
| chr3:98831912-98832515 | Common:2; Rare:102 | ||||
| chr3:98832760-98833095 | Common:3; Rare:49 | ||||
| chr3:98845810-98845970 | Rare:25 | ||||
| chr3:98856501-98856874 | Rare:65 | ||||
| chr3:98872928-98872977 | Rare:7 | ||||
| chr3:98966939-98967158 | Rare:42 | ||||
| chr3:98982348-98982539 | Rare:26 | ||||
| chr3:98986204-98986278 | Rare:14 | ||||
| chr3:100744790-100744965 | Common:3; Rare:51; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:101576879-101576920 | Rare:9 | ||||
| chr3:101676267-101676481 | Common:2; Rare:70 | ||||
| chr3:101940592-101940907 | Common:2; Rare:52 | ||||
| chr3:105408130-105408366 | Common:2; Rare:30 |