| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39107527-39107732 | Common:4; Rare:64 | ||||
| chr3:39383289-39383439 | Common:2; Rare:25; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383544-39383660 | Rare:26; Clinvar:2 | ||||
| chr3:40309515-40309808 | Common:8; Rare:104 | ||||
| chr3:41199404-41199538 | Common:1; Rare:59 | ||||
| chr3:42581879-42582137 | Common:3; Rare:81 | ||||
| chr3:42582272-42582580 | Common:3; Rare:63 | ||||
| chr3:42600532-42600750 | Common:1; Rare:86 | ||||
| chr3:42804435-42804660 | Common:2; Rare:67 | ||||
| chr3:43690792-43691004 | Common:3; Rare:114; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44477645-44477694 | Rare:11 | ||||
| chr3:44624941-44625106 | Common:2; Rare:48 | ||||
| chr3:44761590-44761798 | Common:3; Rare:74 | ||||
| chr3:44976120-44976283 | Common:2; Rare:69 | ||||
| chr3:45026129-45026466 | Common:2; Rare:81 |