| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:172750579-172750794 | Common:3; Rare:62 | ||||
| chr3:173397463-173397796 | Common:4; Rare:105 | ||||
| chr3:174440910-174441007 | Common:1; Rare:26 | ||||
| chr3:177196411-177196563 | Rare:44 | ||||
| chr3:177197129-177197393 | Rare:87 | ||||
| chr3:178536277-178536471 | Rare:31 | ||||
| chr3:179147967-179148126 | Common:1; Rare:40 | ||||
| chr3:179451375-179451722 | Common:2; Rare:120 | ||||
| chr3:179604581-179604903 | Common:3; Rare:138 | ||||
| chr3:180602054-180602258 | Common:1; Rare:72 | ||||
| chr3:180679457-180679544 | Rare:14; Clinvar:3 | ||||
| chr3:180989629-180989851 | Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:183099455-183099717 | Common:2; Rare:84; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183253027-183253288 | Common:3; Rare:79 | ||||
| chr3:183428426-183428718 | Common:1; Rare:81 |