| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43557368-43557481 | Rare:26 | ||||
| chr5:43602601-43602723 | Common:1; Rare:18 | ||||
| chr5:44389240-44389680 | Common:2; Rare:71 | ||||
| chr5:44389700-44389990 | Common:1; Rare:56 | ||||
| chr5:44808706-44808975 | Common:2; Rare:88 | ||||
| chr5:50441361-50441570 | Common:3; Rare:58 | ||||
| chr5:50666690-50667100 | Common:3; Rare:114 | ||||
| chr5:50667748-50667922 | Common:1; Rare:56 | ||||
| chr5:51383260-51383392 | Common:1; Rare:46 | ||||
| chr5:52787690-52788220 | Common:2; Rare:109 | ||||
| chr5:52989191-52989356 | Common:4; Rare:50; Clinvar (benign):1 | ||||
| chr5:52989852-52990252 | Common:4; Rare:141 | ||||
| chr5:53109716-53109917 | Common:1; Rare:104; Clinvar:3 | ||||
| chr5:53480079-53480400 | Rare:75 | ||||
| chr5:53560607-53560719 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 |