| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75131502-75131838 | Common:4; Rare:140 | ||||
| chr17:75146666-75146724 | Common:1; Rare:14 | ||||
| chr17:75205370-75205730 | Common:1; Rare:108 | ||||
| chr17:75261580-75261959 | Common:4; Rare:124; Clinvar (benign):3 | ||||
| chr17:75271142-75271379 | Common:2; Rare:44 | ||||
| chr17:75289358-75289604 | Common:2; Rare:83; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:75393740-75393999 | Common:1; Rare:63 | ||||
| chr17:75456465-75456699 | Rare:71 | ||||
| chr17:75459564-75459738 | Rare:25 | ||||
| chr17:75515449-75515707 | Common:3; Rare:79 | ||||
| chr17:75516394-75516602 | Common:2; Rare:60; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:75525288-75525380 | Rare:18 | ||||
| chr17:75525483-75525811 | Common:3; Rare:105 | ||||
| chr17:75542311-75542469 | Common:2; Rare:32 | ||||
| chr17:75569049-75569255 | Common:6; Rare:80 |