| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15341378-15341581 | Rare:35 | ||||
| chr3:15427471-15427720 | Common:1; Rare:86 | ||||
| chr3:15601460-15602010 | Common:6; Rare:245; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:15859784-15860027 | Common:1; Rare:83 | ||||
| chr3:16174452-16174723 | Common:1; Rare:59 | ||||
| chr3:16264872-16265263 | Common:2; Rare:132 | ||||
| chr3:16513588-16513873 | Common:4; Rare:74 | ||||
| chr3:16884861-16885245 | Common:7; Rare:97 | ||||
| chr3:17742489-17742952 | Common:4; Rare:161 | ||||
| chr3:19946942-19947457 | Common:8; Rare:188 | ||||
| chr3:20186200-20186370 | Common:1; Rare:45 | ||||
| chr3:23202950-23203200 | Rare:84 | ||||
| chr3:23916866-23917204 | Rare:132 | ||||
| chr3:23917573-23918031 | Common:2; Rare:117; Clinvar (benign):1 | ||||
| chr3:24494285-24494317 | Rare:4 |