| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1799770-1799993 | Common:8; Rare:105 | ||||
| chr5:1801278-1801540 | Common:4; Rare:137; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:2751646-2751921 | Common:2; Rare:86 | ||||
| chr5:2751924-2752284 | Common:3; Rare:107 | ||||
| chr5:3595694-3595880 | Common:1; Rare:44 | ||||
| chr5:5140071-5140393 | Common:5; Rare:91 | ||||
| chr5:5422311-5422757 | Common:3; Rare:153 | ||||
| chr5:6378436-6378725 | Rare:112 | ||||
| chr5:6632638-6632875 | Common:3; Rare:99; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr5:6632961-6633471 | Common:8; Rare:159; Clinvar:10; Clinvar (benign):4 | ||||
| chr5:7395578-7396311 | Common:5; Rare:202 | ||||
| chr5:7868991-7869234 | Common:2; Rare:128; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:7899862-7899886 | Rare:10 | ||||
| chr5:9546069-9546313 | Common:6; Rare:55 | ||||
| chr5:10249865-10250553 | Common:19; Rare:316; Clinvar:5; Clinvar (benign):2 |