| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:172750955-172751067 | Rare:30 | ||||
| chr3:173397456-173397810 | Common:4; Rare:116 | ||||
| chr3:174440806-174440992 | Common:2; Rare:54 | ||||
| chr3:177196401-177196763 | Common:2; Rare:120 | ||||
| chr3:177197128-177197391 | Rare:86 | ||||
| chr3:179148079-179148196 | Common:3; Rare:44 | ||||
| chr3:179347636-179347796 | Common:1; Rare:42 | ||||
| chr3:179451381-179451717 | Common:2; Rare:117 | ||||
| chr3:179562658-179563003 | Rare:115 | ||||
| chr3:179604581-179604921 | Common:4; Rare:141 | ||||
| chr3:180601925-180602258 | Common:1; Rare:96 | ||||
| chr3:180912343-180912706 | Common:3; Rare:121 | ||||
| chr3:180989617-180989865 | Rare:97; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:182793344-182793659 | Common:3; Rare:82 | ||||
| chr3:183099451-183099742 | Common:2; Rare:93; Clinvar:3; Clinvar (benign):5 |