| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44123593-44123832 | Common:3; Rare:71 | ||||
| chr17:44186687-44187050 | Common:1; Rare:119 | ||||
| chr17:44187163-44187294 | Rare:34 | ||||
| chr17:44198410-44198545 | Common:2; Rare:29 | ||||
| chr17:44210197-44210357 | Common:2; Rare:47 | ||||
| chr17:44220838-44221057 | Rare:69 | ||||
| chr17:44324771-44324963 | Common:2; Rare:67 | ||||
| chr17:44503374-44503639 | Rare:116 | ||||
| chr17:44899371-44899751 | Common:2; Rare:120; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:45060944-45061365 | Common:3; Rare:118 | ||||
| chr17:45132519-45132639 | Rare:42 | ||||
| chr17:45148275-45148604 | Rare:129 | ||||
| chr17:46923051-46923225 | Common:3; Rare:75; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr17:47189187-47189595 | Common:1; Rare:109 | ||||
| chr17:47323629-47324026 | Common:4; Rare:135 |