| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50783628-50783854 | Common:1; Rare:65 | ||||
| chr3:3126813-3126984 | Common:4; Rare:74; Clinvar (benign):1 | ||||
| chr3:4467235-4467323 | Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4493177-4493348 | Rare:60 | ||||
| chr3:9362966-9363088 | Common:1; Rare:45 | ||||
| chr3:9397437-9397709 | Common:1; Rare:98 | ||||
| chr3:9792414-9792510 | Rare:25 | ||||
| chr3:9792777-9793115 | Common:3; Rare:117 | ||||
| chr3:9916853-9917151 | Common:3; Rare:66 | ||||
| chr3:9933542-9933863 | Common:2; Rare:130; Clinvar:2 | ||||
| chr3:10026315-10026480 | Rare:52 | ||||
| chr3:10115520-10115708 | Common:3; Rare:68 | ||||
| chr3:10321050-10321259 | Common:2; Rare:88 | ||||
| chr3:12484168-12484554 | Common:5; Rare:113; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12664084-12664315 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):2 |