| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69052209-69052443 | Common:4; Rare:82 | ||||
| chr3:81761502-81761728 | Common:7; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:87227244-87227386 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058926-88059294 | Common:3; Rare:135 | ||||
| chr3:88149617-88150063 | Common:5; Rare:138 | ||||
| chr3:94062910-94063040 | Rare:35 | ||||
| chr3:97764704-97764795 | Common:1; Rare:17; Clinvar (benign):1 | ||||
| chr3:98732445-98732512 | Rare:13 | ||||
| chr3:98732619-98732698 | Rare:15 | ||||
| chr3:98901132-98901207 | Common:2; Rare:33 | ||||
| chr3:99638555-99638664 | Rare:24 | ||||
| chr3:99876079-99876278 | Common:2; Rare:56 | ||||
| chr3:100260711-100261057 | Rare:102 | ||||
| chr3:100401407-100401580 | Common:1; Rare:30 | ||||
| chr3:100492474-100492624 | Common:1; Rare:44 |