| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:176326891-176327034 | Common:2; Rare:25 | ||||
| chr3:176327037-176327360 | Common:5; Rare:60 | ||||
| chr3:177394773-177395031 | Common:3; Rare:57 | ||||
| chr3:177670934-177671074 | Common:3; Rare:29 | ||||
| chr3:178207447-178207739 | Common:3; Rare:55 | ||||
| chr3:179260533-179260698 | Common:2; Rare:25 | ||||
| chr3:179524821-179525055 | Common:2; Rare:47 | ||||
| chr3:180948461-180948719 | Common:1; Rare:57 | ||||
| chr3:181610500-181610524 | Rare:4 | ||||
| chr3:181710547-181710669 | Rare:22 | ||||
| chr3:181710996-181711110 | Rare:14 | ||||
| chr3:181712690-181712748 | Rare:14; Clinvar:1 | ||||
| chr3:181713151-181713705 | Common:3; Rare:122; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:181714198-181714288 | Common:1; Rare:14 | ||||
| chr3:181715614-181715912 | Rare:53 |