| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:180989539-180989790 | Rare:107; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:180989801-180989843 | Rare:15 | ||||
| chr3:182793395-182793704 | Common:3; Rare:81 | ||||
| chr3:183099443-183099742 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183697652-183697901 | Common:2; Rare:109 | ||||
| chr3:183884727-183885019 | Rare:113 | ||||
| chr3:184017864-184018109 | Common:1; Rare:77 | ||||
| chr3:184135221-184135391 | Common:2; Rare:51; Clinvar:5 | ||||
| chr3:184154864-184155112 | Rare:43 | ||||
| chr3:184185898-184186209 | Common:4; Rare:112 | ||||
| chr3:184248859-184249032 | Common:1; Rare:91; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249495-184249777 | Common:1; Rare:88 | ||||
| chr3:184298944-184299290 | Common:3; Rare:111 | ||||
| chr3:184314428-184314663 | Common:3; Rare:71 | ||||
| chr3:184362150-184362242 | Common:1; Rare:13 |