| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:21751097-21751411 | Common:4; Rare:100 | ||||
| chr3:23202900-23203207 | Common:1; Rare:105 | ||||
| chr3:23806898-23806998 | Common:1; Rare:28 | ||||
| chr3:23916855-23917204 | Rare:133 | ||||
| chr3:23917586-23918050 | Common:2; Rare:125; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:24494744-24494903 | Rare:43 | ||||
| chr3:24494948-24495293 | Common:4; Rare:95 | ||||
| chr3:25428020-25428081 | Rare:22 | ||||
| chr3:25428106-25428578 | Rare:107 | ||||
| chr3:25783377-25783648 | Common:2; Rare:88; Clinvar (benign):3 | ||||
| chr3:25789966-25790126 | Common:5; Rare:63 | ||||
| chr3:28241441-28241755 | Common:2; Rare:106 | ||||
| chr3:28291732-28291882 | Common:1; Rare:26 | ||||
| chr3:28348612-28348747 | Rare:33 | ||||
| chr3:28348756-28349231 | Common:4; Rare:154 |