| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:18790221-18790499 | Common:5; Rare:96 | ||||
| chr16:18801429-18801919 | Common:4; Rare:164; Clinvar:1 | ||||
| chr16:18925819-18925923 | Rare:37 | ||||
| chr16:18926387-18926792 | Common:3; Rare:138 | ||||
| chr16:19067455-19067723 | Common:6; Rare:115; Clinvar:1 | ||||
| chr16:19067768-19067925 | Common:3; Rare:42 | ||||
| chr16:19521995-19522200 | Rare:51 | ||||
| chr16:19555494-19555729 | Common:1; Rare:110 | ||||
| chr16:20741732-20741996 | Common:1; Rare:114 | ||||
| chr16:20806331-20806659 | Rare:103 | ||||
| chr16:20900219-20900873 | Common:4; Rare:156 | ||||
| chr16:21599360-21599745 | Common:4; Rare:132 | ||||
| chr16:21952991-21953450 | Common:1; Rare:118; Clinvar (benign):3 | ||||
| chr16:22436926-22437077 | Rare:56 | ||||
| chr16:22437370-22437579 | Rare:70 |