| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:2098654-2098957 | Common:4; Rare:120 | ||||
| chr3:4303252-4303412 | Common:1; Rare:63 | ||||
| chr3:4493131-4493572 | Common:2; Rare:146; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:8501638-8501937 | Common:2; Rare:111 | ||||
| chr3:9362988-9363109 | Rare:46 | ||||
| chr3:9397437-9397891 | Common:1; Rare:143 | ||||
| chr3:9731733-9731790 | Common:1; Rare:34 | ||||
| chr3:9749773-9750050 | Common:1; Rare:91 | ||||
| chr3:9769853-9770057 | Common:1; Rare:51 | ||||
| chr3:9792364-9792618 | Rare:70 | ||||
| chr3:9792635-9793115 | Common:4; Rare:162 | ||||
| chr3:9916896-9917202 | Common:4; Rare:65 | ||||
| chr3:9933484-9933863 | Common:2; Rare:155; Clinvar:4 | ||||
| chr3:10026304-10026422 | Rare:40 | ||||
| chr3:10115520-10115737 | Common:3; Rare:80 |