| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:2751636-2751889 | Common:2; Rare:84 | ||||
| chr5:3595595-3595885 | Common:2; Rare:81 | ||||
| chr5:5422140-5422770 | Common:3; Rare:211 | ||||
| chr5:6378518-6378777 | Rare:84 | ||||
| chr5:6632996-6633460 | Common:8; Rare:151; Clinvar:9; Clinvar (benign):4 | ||||
| chr5:6712817-6713103 | Common:4; Rare:97 | ||||
| chr5:6713152-6713518 | Common:3; Rare:121 | ||||
| chr5:6713761-6714401 | Common:3; Rare:210 | ||||
| chr5:7396458-7396669 | Common:1; Rare:61 | ||||
| chr5:7850558-7850869 | Common:3; Rare:47 | ||||
| chr5:7868949-7869221 | Common:2; Rare:144; Clinvar (benign):1 | ||||
| chr5:9546064-9546298 | Common:6; Rare:55 | ||||
| chr5:10249850-10250352 | Common:19; Rare:243; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:10307220-10307420 | Rare:35 | ||||
| chr5:10307525-10307641 | Common:1; Rare:24 |