| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9917039-9917137 | Common:1; Rare:21 | ||||
| chr3:9933511-9933925 | Common:3; Rare:158; Clinvar:3 | ||||
| chr3:9952339-9952535 | Rare:41 | ||||
| chr3:10026295-10026505 | Rare:66 | ||||
| chr3:10115489-10115765 | Common:4; Rare:100 | ||||
| chr3:10141672-10141870 | Common:1; Rare:91; Clinvar:15; Clinvar (benign):18 | ||||
| chr3:10321050-10321297 | Common:2; Rare:101 | ||||
| chr3:11272196-11272437 | Common:2; Rare:59 | ||||
| chr3:11643731-11644088 | Common:2; Rare:94 | ||||
| chr3:11846816-11847052 | Common:1; Rare:71 | ||||
| chr3:12004148-12004409 | Common:5; Rare:64 | ||||
| chr3:12484321-12484560 | Common:5; Rare:81; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12556904-12557173 | Common:5; Rare:93 | ||||
| chr3:12664073-12664330 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:12796592-12796733 | Common:3; Rare:47 |