| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:72955860-72956099 | Common:1; Rare:105 | ||||
| chr5:73448775-73448840 | Rare:12 | ||||
| chr5:73498305-73498693 | Common:3; Rare:130 | ||||
| chr5:73498771-73498793 | Rare:6 | ||||
| chr5:73565365-73565841 | Common:7; Rare:149 | ||||
| chr5:74640494-74640865 | Common:2; Rare:110 | ||||
| chr5:74685054-74685242 | Common:3; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:74767032-74767363 | Common:3; Rare:103 | ||||
| chr5:74768928-74769364 | Common:2; Rare:117 | ||||
| chr5:75511591-75511921 | Common:1; Rare:116 | ||||
| chr5:75717364-75717666 | Common:5; Rare:77 | ||||
| chr5:77087183-77087513 | Rare:49 | ||||
| chr5:78360355-78360683 | Common:5; Rare:128 | ||||
| chr5:78648518-78648529 | Rare:5 | ||||
| chr5:78985785-78985820 | Common:1; Rare:3; Clinvar (benign):1 |