| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160399196-160399308 | Rare:30; Clinvar:1 | ||||
| chr3:160399520-160399669 | Rare:30 | ||||
| chr3:160565564-160565784 | Common:2; Rare:77 | ||||
| chr3:161105290-161105355 | Common:1; Rare:27 | ||||
| chr3:167734825-167735072 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:169663556-169664021 | Common:4; Rare:103 | ||||
| chr3:169773311-169773418 | Rare:34 | ||||
| chr3:169966706-169966851 | Rare:61 | ||||
| chr3:172039485-172039656 | Common:1; Rare:56 | ||||
| chr3:172523393-172523450 | Rare:20 | ||||
| chr3:174440697-174441004 | Common:3; Rare:79 | ||||
| chr3:179147988-179148152 | Common:1; Rare:42 | ||||
| chr3:179604605-179604848 | Common:2; Rare:91 | ||||
| chr3:180601942-180602242 | Common:1; Rare:87 | ||||
| chr3:180912356-180912713 | Common:4; Rare:119 |