| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42536124-42536357 | Common:4; Rare:147; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:42564980-42565250 | Common:2; Rare:80; Clinvar (benign):2 | ||||
| chr17:42566940-42567303 | Common:4; Rare:117 | ||||
| chr17:42577671-42577887 | Common:2; Rare:225 | ||||
| chr17:42609305-42609747 | Common:16; Rare:363; Clinvar (benign):4 | ||||
| chr17:42659184-42659481 | Rare:160 | ||||
| chr17:42682427-42682593 | Rare:38 | ||||
| chr17:42744490-42744860 | Rare:127 | ||||
| chr17:42745006-42745144 | Common:4; Rare:96 | ||||
| chr17:42760340-42760850 | Common:9; Rare:246 | ||||
| chr17:42760880-42761254 | Rare:138 | ||||
| chr17:42761250-42761850 | Common:3; Rare:154 | ||||
| chr17:42773368-42773538 | Rare:86 | ||||
| chr17:42779849-42780251 | Common:5; Rare:142 | ||||
| chr17:42780407-42780714 | Common:6; Rare:181; Clinvar:1; Clinvar (benign):1 |