| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44141769-44141979 | Common:1; Rare:48 | ||||
| chr17:44186629-44187002 | Common:1; Rare:134 | ||||
| chr17:44187174-44187274 | Rare:29 | ||||
| chr17:44221214-44221356 | Rare:42 | ||||
| chr17:44324765-44324997 | Common:2; Rare:84 | ||||
| chr17:44345072-44345334 | Rare:57; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:44350506-44350733 | Rare:77; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:44350795-44351093 | Rare:99; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr17:44503332-44503719 | Rare:146 | ||||
| chr17:44708529-44708899 | Common:4; Rare:100 | ||||
| chr17:44830206-44830362 | Common:1; Rare:81 | ||||
| chr17:44898975-44899137 | Common:1; Rare:40 | ||||
| chr17:44899367-44899741 | Common:2; Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:44947641-44947901 | Common:1; Rare:66 | ||||
| chr17:45051420-45051691 | Common:1; Rare:88 |