| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75109785-75110156 | Common:7; Rare:212 | ||||
| chr17:75130630-75131136 | Common:10; Rare:480 | ||||
| chr17:75131360-75131908 | Common:15; Rare:520 | ||||
| chr17:75154383-75154526 | Rare:73 | ||||
| chr17:75154470-75154832 | Common:2; Rare:198 | ||||
| chr17:75182501-75182715 | Common:6; Rare:156 | ||||
| chr17:75182839-75183280 | Common:5; Rare:357 | ||||
| chr17:75205135-75205797 | Common:4; Rare:508 | ||||
| chr17:75261489-75262034 | Common:26; Rare:520; Clinvar (benign):12 | ||||
| chr17:75262319-75263006 | Common:6; Rare:354; Clinvar (benign):4 | ||||
| chr17:75270361-75270882 | Rare:209 | ||||
| chr17:75271075-75271499 | Common:12; Rare:193 | ||||
| chr17:75288714-75289114 | Common:1; Rare:101 | ||||
| chr17:75289305-75289721 | Common:8; Rare:320; Clinvar:3; Clinvar (benign):6 | ||||
| chr17:75393677-75394146 | Common:3; Rare:298 |