| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44186695-44187250 | Rare:161 | ||||
| chr17:44221273-44221427 | Rare:46 | ||||
| chr17:44324781-44324976 | Common:2; Rare:71 | ||||
| chr17:44503377-44503674 | Rare:127 | ||||
| chr17:44899383-44899729 | Common:2; Rare:108; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:45060993-45061329 | Common:2; Rare:88 | ||||
| chr17:45148156-45148479 | Common:1; Rare:94 | ||||
| chr17:48048084-48048391 | Rare:73 | ||||
| chr17:50186638-50187129 | Common:2; Rare:144; Clinvar:8; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr17:50187166-50187548 | Common:2; Rare:68; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:50188298-50189024 | Common:2; Rare:178; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
| chr17:50189064-50189540 | Rare:109; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:50192460-50192717 | Common:1; Rare:63; Clinvar:4; Clinvar (benign):8 | ||||
| chr17:50192889-50193171 | Common:3; Rare:72; Clinvar:1; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:50194571-50194860 | Common:2; Rare:86; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):5 |