| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:15856982-15857151 | Common:2; Rare:38; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:15888587-15888815 | Common:2; Rare:82 | ||||
| chr16:18790287-18790490 | Common:1; Rare:73 | ||||
| chr16:18801443-18801774 | Common:2; Rare:115 | ||||
| chr16:18926397-18926605 | Common:2; Rare:92 | ||||
| chr16:19067455-19067702 | Common:5; Rare:104; Clinvar:1 | ||||
| chr16:19067789-19067929 | Common:2; Rare:36 | ||||
| chr16:19521995-19522191 | Rare:49 | ||||
| chr16:19862014-19862132 | Rare:24 | ||||
| chr16:20806349-20806542 | Rare:72 | ||||
| chr16:20900301-20900843 | Common:4; Rare:128 | ||||
| chr16:21283811-21283888 | Common:1; Rare:17 | ||||
| chr16:21953028-21953435 | Common:1; Rare:102; Clinvar (benign):3 | ||||
| chr16:22297186-22297454 | Common:3; Rare:138 | ||||
| chr16:22437103-22437296 | Rare:66 |