| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30064338-30064486 | Common:1; Rare:27; Clinvar (benign):1 | ||||
| chr16:30065566-30065853 | Rare:100 | ||||
| chr16:30069559-30069976 | Common:1; Rare:157; Clinvar:6; Clinvar (benign):6 | ||||
| chr16:30075894-30076059 | Common:1; Rare:56 | ||||
| chr16:30122940-30123369 | Common:7; Rare:122 | ||||
| chr16:30355210-30355434 | Common:1; Rare:78 | ||||
| chr16:30355813-30355947 | Common:1; Rare:31 | ||||
| chr16:30407523-30407645 | Rare:43 | ||||
| chr16:30534867-30535107 | Common:3; Rare:81 | ||||
| chr16:30585561-30585897 | Common:1; Rare:73 | ||||
| chr16:30650481-30650782 | Rare:60 | ||||
| chr16:30697933-30698235 | Common:1; Rare:134 | ||||
| chr16:30698457-30698640 | Common:1; Rare:70 | ||||
| chr16:30699003-30699386 | Rare:100; Clinvar (benign):1 | ||||
| chr16:30748125-30748473 | Common:2; Rare:86; Clinvar:2; Clinvar (benign):1 |