| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9792777-9793123 | Common:3; Rare:121 | ||||
| chr3:10026370-10026438 | Rare:18 | ||||
| chr3:11225881-11226016 | Rare:16 | ||||
| chr3:12484336-12484511 | Common:4; Rare:53; Clinvar (benign):1 | ||||
| chr3:12664088-12664315 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:14124728-14125089 | Common:4; Rare:104; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178569-14178870 | Common:2; Rare:155; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14947418-14947554 | Common:2; Rare:69 | ||||
| chr3:15427501-15427629 | Rare:42 | ||||
| chr3:15601539-15601756 | Common:3; Rare:84 | ||||
| chr3:16264897-16265221 | Common:2; Rare:98 | ||||
| chr3:20186204-20186355 | Common:1; Rare:42 | ||||
| chr3:23916916-23917186 | Rare:101 | ||||
| chr3:25783391-25783640 | Common:2; Rare:77; Clinvar (benign):3 | ||||
| chr3:28348773-28349178 | Common:3; Rare:130 |