| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30762080-30762343 | Common:3; Rare:89 | ||||
| chr16:30893940-30894252 | Common:5; Rare:84 | ||||
| chr16:31074187-31074450 | Common:1; Rare:73 | ||||
| chr16:31471907-31472189 | Rare:65 | ||||
| chr16:31508374-31508424 | Rare:23 | ||||
| chr16:46689134-46689384 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973568-46973768 | Rare:86 | ||||
| chr16:47461027-47461365 | Common:2; Rare:127; Clinvar (benign):2 | ||||
| chr16:48244257-48244391 | Common:2; Rare:47 | ||||
| chr16:53703815-53704187 | Rare:109; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:54286722-54286997 | Common:1; Rare:83 | ||||
| chr16:55479408-55479499 | Common:1; Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:56451287-56451600 | Common:1; Rare:99 | ||||
| chr16:56608280-56608776 | Common:4; Rare:139 | ||||
| chr16:56729974-56730204 | Common:1; Rare:53 |