| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4767135-4767352 | Common:1; Rare:74 | ||||
| chr16:4847244-4847511 | Common:3; Rare:125 | ||||
| chr16:4847913-4848209 | Common:2; Rare:98 | ||||
| chr16:4958008-4958330 | Common:8; Rare:87 | ||||
| chr16:5033885-5033992 | Rare:50 | ||||
| chr16:5097768-5097952 | Common:4; Rare:59 | ||||
| chr16:8590272-8590575 | Rare:65 | ||||
| chr16:8621585-8621772 | Common:1; Rare:73 | ||||
| chr16:8674419-8674661 | Common:1; Rare:87; Clinvar:2 | ||||
| chr16:8797606-8797937 | Common:1; Rare:136; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr16:8868961-8869299 | Common:5; Rare:148 | ||||
| chr16:10580065-10580139 | Rare:16 | ||||
| chr16:10580565-10580768 | Rare:63 | ||||
| chr16:10743723-10743875 | Rare:63 | ||||
| chr16:10744061-10744317 | Common:1; Rare:95 |