| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46789875-46790144 | Common:5; Rare:67 | ||||
| chr16:46831103-46831342 | Common:2; Rare:89 | ||||
| chr16:46831345-46831610 | Common:1; Rare:76 | ||||
| chr16:46883807-46884452 | Common:3; Rare:162 | ||||
| chr16:46972558-46972694 | Common:1; Rare:32 | ||||
| chr16:46972884-46973000 | Common:1; Rare:31 | ||||
| chr16:46973008-46973385 | Rare:102 | ||||
| chr16:46973569-46973980 | Common:1; Rare:149 | ||||
| chr16:46973983-46974052 | Common:1; Rare:14 | ||||
| chr16:47143120-47143246 | Rare:26 | ||||
| chr16:47143438-47143626 | Rare:54 | ||||
| chr16:47143896-47144145 | Rare:116 | ||||
| chr16:47144246-47144321 | Rare:17 | ||||
| chr16:47144432-47144693 | Rare:63 | ||||
| chr16:47460965-47461426 | Common:3; Rare:187; Clinvar (benign):3 |