| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15427465-15427635 | Common:1; Rare:61 | ||||
| chr3:15601460-15601823 | Common:5; Rare:150; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:15859800-15860114 | Common:4; Rare:97 | ||||
| chr3:16174522-16175068 | Common:1; Rare:120 | ||||
| chr3:16175070-16175573 | Common:2; Rare:149 | ||||
| chr3:16264872-16265229 | Common:2; Rare:117 | ||||
| chr3:16512886-16513038 | Common:1; Rare:26 | ||||
| chr3:17742520-17742943 | Common:4; Rare:150 | ||||
| chr3:18424197-18424299 | Common:1; Rare:19 | ||||
| chr3:19946974-19947475 | Common:7; Rare:185 | ||||
| chr3:21751086-21751434 | Common:4; Rare:112 | ||||
| chr3:23916855-23917224 | Rare:139 | ||||
| chr3:24494736-24494903 | Rare:44 | ||||
| chr3:25427939-25428071 | Rare:33 | ||||
| chr3:25428103-25428398 | Rare:67 |