| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89918565-89918879 | Common:4; Rare:97; Clinvar:3; Clinvar (benign):5 | ||||
| chr16:89921804-89921949 | Rare:40 | ||||
| chr16:89923132-89923393 | Rare:116 | ||||
| chr16:89972468-89972658 | Common:1; Rare:67 | ||||
| chr16:90022581-90022697 | Rare:46 | ||||
| chr17:714792-714891 | Common:2; Rare:35 | ||||
| chr17:732301-732596 | Common:1; Rare:104 | ||||
| chr17:1400048-1400381 | Common:3; Rare:141 | ||||
| chr17:1491615-1491827 | Common:1; Rare:66 | ||||
| chr17:1516588-1516960 | Common:2; Rare:130 | ||||
| chr17:1653547-1653873 | Common:3; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:1716172-1716534 | Common:3; Rare:114 | ||||
| chr17:1783415-1783623 | Rare:71 | ||||
| chr17:1829780-1830062 | Common:8; Rare:118 | ||||
| chr17:2214311-2214424 | Common:1; Rare:18 |