| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:19362565-19362773 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:19377896-19377988 | Common:1; Rare:22 | ||||
| chr17:19378162-19378570 | Common:2; Rare:98 | ||||
| chr17:19648592-19648984 | Common:4; Rare:133 | ||||
| chr17:20009243-20009383 | Common:2; Rare:42 | ||||
| chr17:20155802-20156117 | Common:1; Rare:100 | ||||
| chr17:20868211-20868527 | Common:2; Rare:75 | ||||
| chr17:21011214-21011419 | Common:2; Rare:38 | ||||
| chr17:21214148-21214348 | Common:2; Rare:90 | ||||
| chr17:27293992-27294126 | Common:1; Rare:56 | ||||
| chr17:28318924-28319251 | Common:3; Rare:115 | ||||
| chr17:28319285-28319344 | Rare:20 | ||||
| chr17:28335376-28335824 | Common:1; Rare:108 | ||||
| chr17:28357454-28357667 | Common:5; Rare:106 | ||||
| chr17:28552534-28552736 | Rare:77; Clinvar:3; Clinvar (benign):1 |