| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50055681-50056306 | Common:14; Rare:271 | ||||
| chr17:50095060-50095450 | Common:4; Rare:234 | ||||
| chr17:50149500-50150279 | Common:16; Rare:243; Clinvar:9 | ||||
| chr17:50150974-50151251 | Rare:104 | ||||
| chr17:50199654-50200130 | Common:7; Rare:242; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr17:50200174-50200511 | Common:8; Rare:128; Clinvar:2 | ||||
| chr17:50274275-50274515 | Common:2; Rare:98 | ||||
| chr17:50345923-50346169 | Common:8; Rare:158 | ||||
| chr17:50372830-50373284 | Common:9; Rare:247 | ||||
| chr17:50397442-50397607 | Common:1; Rare:51 | ||||
| chr17:50426102-50426279 | Common:2; Rare:83 | ||||
| chr17:50478708-50478868 | Common:2; Rare:87 | ||||
| chr17:50478890-50479180 | Common:1; Rare:142 | ||||
| chr17:50634569-50635140 | Common:5; Rare:162 | ||||
| chr17:50668319-50668444 | Common:1; Rare:29 |