| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14947219-14947608 | Common:4; Rare:171 | ||||
| chr3:15205982-15206270 | Rare:103 | ||||
| chr3:15427465-15427679 | Common:1; Rare:75 | ||||
| chr3:15601499-15601804 | Common:4; Rare:126; Clinvar:1 | ||||
| chr3:15859831-15860130 | Common:4; Rare:99 | ||||
| chr3:16264921-16265229 | Common:2; Rare:85 | ||||
| chr3:17742591-17742952 | Common:4; Rare:127 | ||||
| chr3:19946974-19947450 | Common:7; Rare:177 | ||||
| chr3:23202926-23203126 | Common:1; Rare:74 | ||||
| chr3:23916911-23917196 | Rare:108 | ||||
| chr3:23917621-23917967 | Common:2; Rare:92; Clinvar (benign):1 | ||||
| chr3:24494744-24494903 | Rare:43 | ||||
| chr3:25783386-25783621 | Common:2; Rare:78; Clinvar (benign):3 | ||||
| chr3:25789977-25790106 | Common:2; Rare:50 | ||||
| chr3:28348784-28348859 | Rare:24 |