| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9916869-9917156 | Common:3; Rare:66 | ||||
| chr3:9933544-9933857 | Common:2; Rare:125; Clinvar:2 | ||||
| chr3:10026334-10026480 | Rare:42 | ||||
| chr3:10141678-10141962 | Common:1; Rare:134; Clinvar:34; Clinvar (benign):28 | ||||
| chr3:10321048-10321150 | Common:1; Rare:58 | ||||
| chr3:11225903-11225995 | Rare:11 | ||||
| chr3:11272240-11272425 | Common:1; Rare:41 | ||||
| chr3:11643818-11644016 | Common:2; Rare:59 | ||||
| chr3:12484396-12484522 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:12663526-12663817 | Common:7; Rare:80; Clinvar:1 | ||||
| chr3:12664077-12664300 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:12759253-12759518 | Common:4; Rare:57 | ||||
| chr3:13420226-13420438 | Common:1; Rare:59 | ||||
| chr3:13480040-13480339 | Common:2; Rare:70 | ||||
| chr3:14124697-14125184 | Common:4; Rare:143; Clinvar:4; Clinvar (benign):1 |