| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75261590-75261920 | Common:4; Rare:101; Clinvar (benign):1 | ||||
| chr17:75271146-75271356 | Common:2; Rare:38 | ||||
| chr17:75393742-75394070 | Common:1; Rare:74 | ||||
| chr17:75515423-75515736 | Common:3; Rare:92 | ||||
| chr17:75667147-75667378 | Common:4; Rare:70 | ||||
| chr17:75784586-75784872 | Common:2; Rare:125 | ||||
| chr17:75979045-75979283 | Rare:66; Clinvar:4 | ||||
| chr17:75979381-75979488 | Common:1; Rare:28; Clinvar (benign):1 | ||||
| chr17:76103696-76103867 | Common:5; Rare:60 | ||||
| chr17:76501380-76501579 | Rare:66; Clinvar (benign):3 | ||||
| chr17:76688619-76688846 | Common:4; Rare:48 | ||||
| chr17:76725773-76726076 | Common:1; Rare:83 | ||||
| chr17:76726491-76726886 | Common:5; Rare:146 | ||||
| chr17:76737309-76737537 | Common:3; Rare:91 | ||||
| chr17:76737880-76738121 | Common:4; Rare:69 |