| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50627560-50627751 | Common:1; Rare:37 | ||||
| chr3:51991296-51991357 | Rare:23 | ||||
| chr3:52694884-52695199 | Common:2; Rare:90 | ||||
| chr3:57557403-57557589 | Rare:56 | ||||
| chr3:57583921-57584276 | Common:1; Rare:73 | ||||
| chr3:58428525-58428696 | Common:2; Rare:36; Clinvar:1 | ||||
| chr3:61743136-61743396 | Common:3; Rare:52 | ||||
| chr3:64685075-64685151 | Rare:23 | ||||
| chr3:73521145-73521438 | Rare:57 | ||||
| chr3:75435024-75435388 | Common:5; Rare:124 | ||||
| chr3:75641103-75641397 | Common:1; Rare:47 | ||||
| chr3:75670142-75670282 | |||||
| chr3:81761459-81761659 | Common:7; Rare:77; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:101576948-101577041 | Common:1; Rare:25 | ||||
| chr3:101676282-101676509 | Common:1; Rare:77 |