| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48048606-48048795 | Common:3; Rare:25 | ||||
| chr17:48101388-48101513 | Common:2; Rare:40 | ||||
| chr17:48944754-48944886 | Common:1; Rare:50 | ||||
| chr17:50373174-50373235 | Common:1; Rare:24 | ||||
| chr17:54968619-54968766 | Common:3; Rare:74 | ||||
| chr17:59106734-59106993 | Common:2; Rare:85; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:59155168-59155462 | Common:2; Rare:70 | ||||
| chr17:59619590-59619944 | Common:3; Rare:125 | ||||
| chr17:59707402-59707700 | Common:3; Rare:83; Clinvar (benign):2 | ||||
| chr17:63773551-63773852 | Common:2; Rare:99 | ||||
| chr17:73232263-73232707 | Common:3; Rare:150 | ||||
| chr17:75261590-75261925 | Common:4; Rare:102; Clinvar (benign):1 | ||||
| chr17:75667152-75667372 | Common:4; Rare:68 | ||||
| chr17:75979150-75979271 | Rare:31; Clinvar:3 | ||||
| chr17:76726567-76726884 | Common:5; Rare:119 |