| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:159839821-159840172 | Common:3; Rare:77 | ||||
| chr3:160399175-160399307 | Rare:35; Clinvar:2 | ||||
| chr3:160399498-160399678 | Rare:46; Clinvar:1 | ||||
| chr3:160449796-160449876 | Common:1; Rare:25 | ||||
| chr3:160565406-160565797 | Common:2; Rare:147 | ||||
| chr3:160755442-160755686 | Common:1; Rare:88 | ||||
| chr3:161105025-161105384 | Common:4; Rare:105 | ||||
| chr3:161221184-161221356 | Common:2; Rare:59 | ||||
| chr3:167734799-167735297 | Common:5; Rare:164; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735586-167735794 | Rare:57; Clinvar:1 | ||||
| chr3:169772666-169772837 | Common:1; Rare:42 | ||||
| chr3:169773331-169773459 | Common:1; Rare:41 | ||||
| chr3:169966603-169967123 | Common:7; Rare:162 | ||||
| chr3:170222296-170222553 | Common:2; Rare:81 | ||||
| chr3:170358205-170358464 | Common:3; Rare:93 |