| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9986768-9987153 | Common:4; Rare:111 | ||||
| chr3:10026287-10026480 | Rare:63 | ||||
| chr3:10141655-10142000 | Common:2; Rare:162; Clinvar:39; Clinvar (benign):33 | ||||
| chr3:11154338-11154542 | Common:4; Rare:53 | ||||
| chr3:11225837-11226027 | Rare:32 | ||||
| chr3:11719419-11719548 | Rare:42 | ||||
| chr3:11720686-11720867 | Rare:28 | ||||
| chr3:12158857-12159023 | Rare:53 | ||||
| chr3:12287747-12287995 | Common:7; Rare:44 | ||||
| chr3:12288927-12289086 | Common:1; Rare:35 | ||||
| chr3:12484293-12484570 | Common:5; Rare:93; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12545507-12545824 | Common:3; Rare:64 | ||||
| chr3:12664077-12664330 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:13420177-13420464 | Common:1; Rare:89 | ||||
| chr3:13480016-13480334 | Common:3; Rare:80 |