| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:92897926-92898045 | Common:1; Rare:27 | ||||
| chr15:101275949-101276223 | Common:3; Rare:56 | ||||
| chr15:101281262-101281517 | Common:3; Rare:49 | ||||
| chr16:89751-90036 | Common:1; Rare:99; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:192329-192460 | Common:1; Rare:30 | ||||
| chr16:368329-368566 | Common:2; Rare:110; Clinvar (benign):1 | ||||
| chr16:399377-399736 | Common:4; Rare:139 | ||||
| chr16:634454-634800 | Common:1; Rare:138 | ||||
| chr16:634898-635201 | Rare:91 | ||||
| chr16:647778-648151 | Common:2; Rare:120 | ||||
| chr16:2252945-2253226 | Common:1; Rare:71 | ||||
| chr16:2603293-2603582 | Common:2; Rare:128 | ||||
| chr16:2673354-2673715 | Common:10; Rare:126 | ||||
| chr16:2868179-2868378 | Common:2; Rare:58 | ||||
| chr16:3021210-3021997 | Common:4; Rare:249 |