| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179451367-179451717 | Common:2; Rare:122 | ||||
| chr3:179604601-179604857 | Common:2; Rare:102 | ||||
| chr3:180602020-180602242 | Common:1; Rare:73 | ||||
| chr3:180989617-180989833 | Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:182980491-182980768 | Common:1; Rare:95 | ||||
| chr3:183099443-183099742 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183254060-183254178 | Common:1; Rare:32 | ||||
| chr3:183265078-183265328 | Rare:42 | ||||
| chr3:183635507-183635716 | Common:3; Rare:63 | ||||
| chr3:183697647-183697904 | Common:2; Rare:110 | ||||
| chr3:184017876-184018073 | Common:1; Rare:58 | ||||
| chr3:184135221-184135385 | Common:2; Rare:48; Clinvar:5 | ||||
| chr3:184180431-184180642 | Common:2; Rare:57 | ||||
| chr3:184185861-184186210 | Common:5; Rare:131 | ||||
| chr3:184248891-184249029 | Rare:69; Clinvar:5; Clinvar (benign):1 |