| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44708576-44708699 | Common:1; Rare:25 | ||||
| chr17:44708730-44708919 | Common:6; Rare:119 | ||||
| chr17:44775615-44776015 | Common:7; Rare:123 | ||||
| chr17:44899340-44899741 | Common:4; Rare:237; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44947647-44947911 | Common:2; Rare:136 | ||||
| chr17:45051351-45052151 | Common:10; Rare:264 | ||||
| chr17:45060912-45061461 | Common:6; Rare:308 | ||||
| chr17:45132476-45132667 | Common:3; Rare:114 | ||||
| chr17:45148122-45148499 | Common:2; Rare:217 | ||||
| chr17:45160934-45161123 | Rare:81 | ||||
| chr17:45161459-45162004 | Common:2; Rare:261 | ||||
| chr17:45316975-45317293 | Common:5; Rare:90 | ||||
| chr17:45490681-45490913 | Common:2; Rare:142 | ||||
| chr17:45894247-45894618 | Common:6; Rare:216; Clinvar:8; Clinvar (benign):4 | ||||
| chr17:46193264-46193600 | Common:12; Rare:165 |