| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69084755-69085063 | Common:3; Rare:78 | ||||
| chr3:71581943-71582387 | Common:1; Rare:126 | ||||
| chr3:81761515-81761698 | Common:7; Rare:64; Clinvar (benign):1 | ||||
| chr3:87227186-87227375 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058923-88059294 | Common:3; Rare:137 | ||||
| chr3:88149617-88150027 | Rare:115 | ||||
| chr3:94062897-94063089 | Rare:46 | ||||
| chr3:97764491-97764793 | Common:1; Rare:65; Clinvar (benign):1 | ||||
| chr3:98522858-98523105 | Common:1; Rare:76 | ||||
| chr3:99817553-99817900 | Rare:101 | ||||
| chr3:100260688-100261039 | Rare:97 | ||||
| chr3:100334666-100334784 | Common:1; Rare:56 | ||||
| chr3:100401441-100401582 | Rare:21 | ||||
| chr3:100709300-100709639 | Common:5; Rare:107; Clinvar (benign):1 | ||||
| chr3:101513135-101513343 | Common:8; Rare:43 |