| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:641759-641950 | Common:3; Rare:64 | ||||
| chr16:649077-649375 | Common:1; Rare:92 | ||||
| chr16:680318-680472 | Common:2; Rare:50 | ||||
| chr16:681153-681550 | Rare:128; Clinvar:1; Clinvar (pathogenic):5 | ||||
| chr16:684326-684475 | Common:3; Rare:81 | ||||
| chr16:690346-690548 | Common:3; Rare:83 | ||||
| chr16:726848-727126 | Common:4; Rare:73 | ||||
| chr16:1230091-1230363 | Common:2; Rare:59 | ||||
| chr16:1414681-1414919 | Common:5; Rare:65 | ||||
| chr16:1420712-1420939 | Common:1; Rare:93 | ||||
| chr16:1493241-1493392 | Common:1; Rare:59 | ||||
| chr16:1533484-1533778 | Common:1; Rare:58 | ||||
| chr16:1612037-1612335 | Common:1; Rare:97; Clinvar:1 | ||||
| chr16:1706030-1706378 | Common:3; Rare:115 | ||||
| chr16:1771495-1771848 | Common:3; Rare:140 |