| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43778894-43779076 | Rare:43 | ||||
| chr17:44070612-44070930 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44123596-44123797 | Common:3; Rare:61 | ||||
| chr17:44186608-44187013 | Common:2; Rare:145 | ||||
| chr17:44187177-44187274 | Rare:27 | ||||
| chr17:44209367-44209705 | Rare:84 | ||||
| chr17:44210801-44211141 | Common:1; Rare:98 | ||||
| chr17:44220797-44221337 | Common:1; Rare:176 | ||||
| chr17:44222077-44222255 | Rare:38 | ||||
| chr17:44268029-44268438 | Rare:80; Clinvar:3 | ||||
| chr17:44321431-44321708 | Common:2; Rare:117 | ||||
| chr17:44324748-44325023 | Common:3; Rare:99 | ||||
| chr17:44350795-44351129 | Rare:108; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr17:44503335-44503714 | Rare:143 | ||||
| chr17:44899375-44899735 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):1 |