| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4682614-4682886 | Rare:102 | ||||
| chr16:4850323-4850405 | Rare:23 | ||||
| chr16:8859283-8859423 | Common:1; Rare:80 | ||||
| chr16:9092815-9092998 | Common:2; Rare:69 | ||||
| chr16:10888432-10888538 | Common:2; Rare:23 | ||||
| chr16:10895469-10895764 | Common:4; Rare:82; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:11670506-11670667 | Common:1; Rare:36 | ||||
| chr16:11700472-11700663 | Rare:52 | ||||
| chr16:15029755-15030007 | Common:2; Rare:45 | ||||
| chr16:15590933-15591214 | Common:1; Rare:67 | ||||
| chr16:15611003-15611251 | Common:2; Rare:66 | ||||
| chr16:15636263-15636463 | Common:1; Rare:52 | ||||
| chr16:15715162-15715376 | Common:1; Rare:57; Clinvar:4; Clinvar (benign):8 | ||||
| chr16:15719275-15719552 | Common:2; Rare:84; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:15735555-15735765 | Common:4; Rare:52; Clinvar:2; Clinvar (benign):3 |