| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9792732-9793115 | Common:3; Rare:131 | ||||
| chr3:9933585-9933863 | Common:1; Rare:105 | ||||
| chr3:10026356-10026443 | Rare:21 | ||||
| chr3:11272190-11272413 | Common:2; Rare:52 | ||||
| chr3:11719453-11719575 | Rare:35 | ||||
| chr3:12287697-12287961 | Common:7; Rare:57 | ||||
| chr3:12288975-12289075 | Rare:17 | ||||
| chr3:12664081-12664287 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:13480040-13480306 | Common:2; Rare:60 | ||||
| chr3:14124728-14125145 | Common:4; Rare:117; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178569-14178861 | Common:2; Rare:150; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14402350-14402636 | Common:1; Rare:78 | ||||
| chr3:14947377-14947549 | Common:3; Rare:82 | ||||
| chr3:15206060-15206314 | Common:1; Rare:101 | ||||
| chr3:15427498-15427623 | Rare:45 |