| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:74701096-74701343 | Common:2; Rare:50 | ||||
| chr16:75305413-75305742 | Rare:53 | ||||
| chr16:75433363-75433852 | Common:4; Rare:159 | ||||
| chr16:75464352-75464470 | Common:4; Rare:58 | ||||
| chr16:75556211-75556394 | Common:2; Rare:70; Clinvar (benign):4 | ||||
| chr16:75647614-75647817 | Common:2; Rare:102; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648087-75648207 | Rare:51 | ||||
| chr16:75648636-75648667 | Rare:14 | ||||
| chr16:77190702-77191010 | Common:10; Rare:101 | ||||
| chr16:77191086-77191221 | Common:2; Rare:57 | ||||
| chr16:78099539-78099731 | Common:1; Rare:81 | ||||
| chr16:81006798-81007277 | Common:5; Rare:162 | ||||
| chr16:81077203-81077319 | Common:1; Rare:54 | ||||
| chr16:81181318-81181501 | Common:1; Rare:51 | ||||
| chr16:81314781-81315077 | Common:3; Rare:140; Clinvar:4; Clinvar (benign):1 |