| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:4303252-4303424 | Common:1; Rare:67 | ||||
| chr3:4303506-4303658 | Common:1; Rare:52 | ||||
| chr3:4493165-4493532 | Rare:125; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4979180-4979559 | Common:2; Rare:86 | ||||
| chr3:8501638-8501941 | Common:2; Rare:111 | ||||
| chr3:9362972-9363109 | Common:1; Rare:51 | ||||
| chr3:9397436-9397824 | Common:1; Rare:131 | ||||
| chr3:9749818-9749974 | Rare:48 | ||||
| chr3:9769857-9770070 | Common:1; Rare:53 | ||||
| chr3:9792388-9792611 | Rare:58 | ||||
| chr3:9792705-9793123 | Common:3; Rare:148 | ||||
| chr3:9843975-9844112 | Common:2; Rare:57 | ||||
| chr3:9878774-9879225 | Common:2; Rare:75 | ||||
| chr3:9880217-9880360 | Rare:22 | ||||
| chr3:9890481-9890683 | Common:2; Rare:77 |