| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44186658-44187002 | Common:1; Rare:127 | ||||
| chr17:44187142-44187283 | Rare:38 | ||||
| chr17:44220845-44220978 | Rare:37 | ||||
| chr17:44221273-44221443 | Rare:48 | ||||
| chr17:44324771-44324997 | Common:2; Rare:81 | ||||
| chr17:44344997-44345327 | Common:1; Rare:71; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:44350506-44350748 | Rare:83; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:44352111-44352571 | Common:1; Rare:154; Clinvar:14; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr17:44503366-44503649 | Rare:120 | ||||
| chr17:44899367-44899479 | Rare:47 | ||||
| chr17:44899596-44899769 | Common:2; Rare:48; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:45060958-45061339 | Common:3; Rare:98 | ||||
| chr17:45092994-45093168 | Common:1; Rare:31 | ||||
| chr17:45132331-45132644 | Common:2; Rare:94 | ||||
| chr17:45148154-45148602 | Common:1; Rare:153 |