| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:167734832-167735210 | Common:3; Rare:117; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:169773331-169773418 | Rare:25 | ||||
| chr3:169966610-169966854 | Common:2; Rare:91 | ||||
| chr3:170870166-170870359 | Rare:86 | ||||
| chr3:171026687-171026864 | Rare:37; Clinvar:1 | ||||
| chr3:171460372-171460581 | Rare:50 | ||||
| chr3:179604628-179604838 | Common:1; Rare:70 | ||||
| chr3:180602020-180602242 | Common:1; Rare:73 | ||||
| chr3:180989629-180989770 | Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:183099444-183099717 | Common:2; Rare:90; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183884822-183885044 | Common:2; Rare:77 | ||||
| chr3:184135212-184135385 | Common:2; Rare:49; Clinvar:5 | ||||
| chr3:184185856-184186203 | Common:5; Rare:129 | ||||
| chr3:184249527-184249689 | Rare:44 | ||||
| chr3:184298964-184299272 | Common:2; Rare:92 |