| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4734056-4734425 | Common:1; Rare:141 | ||||
| chr16:4734624-4735044 | Common:3; Rare:120 | ||||
| chr16:4767068-4767419 | Common:2; Rare:111 | ||||
| chr16:4800427-4800623 | Rare:96; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr16:4802126-4802461 | Common:1; Rare:176; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr16:4802622-4802764 | Rare:49; Clinvar:4 | ||||
| chr16:4802900-4803110 | Common:3; Rare:99; Clinvar:2 | ||||
| chr16:4847046-4847067 | Rare:7 | ||||
| chr16:4847187-4847766 | Common:4; Rare:260 | ||||
| chr16:4848220-4848354 | Common:2; Rare:41 | ||||
| chr16:5033579-5033702 | Common:1; Rare:64 | ||||
| chr16:5033847-5034023 | Rare:73 | ||||
| chr16:5071655-5071987 | Common:1; Rare:158; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:5072027-5072387 | Common:5; Rare:102; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:5097680-5097992 | Common:4; Rare:123 |