Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:75109880-75109969 | Common:1; Rare:22 | ||||
chr17:75130797-75131093 | Common:2; Rare:103 | ||||
chr17:75205370-75205734 | Common:1; Rare:110 | ||||
chr17:75261590-75261962 | Common:4; Rare:124; Clinvar (benign):3 | ||||
chr17:75289420-75289651 | Common:1; Rare:67; Clinvar:1 | ||||
chr17:75393747-75394023 | Common:1; Rare:66 | ||||
chr17:75667136-75667378 | Common:4; Rare:76 | ||||
chr17:75784558-75784872 | Common:2; Rare:138 | ||||
chr17:75904868-75905032 | Common:2; Rare:55 | ||||
chr17:75979084-75979283 | Rare:54; Clinvar:4 | ||||
chr17:76103712-76103867 | Common:4; Rare:49 | ||||
chr17:76353888-76354096 | Rare:64 | ||||
chr17:76501402-76501579 | Rare:55; Clinvar (benign):3 | ||||
chr17:76726487-76726882 | Common:5; Rare:145 | ||||
chr17:76737325-76737582 | Common:2; Rare:94 |