| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:100919229-100919383 | Common:1; Rare:50 | ||||
| chr15:101277405-101277630 | Common:3; Rare:121 | ||||
| chr15:101295193-101295403 | Common:1; Rare:67 | ||||
| chr15:101652271-101652493 | Common:4; Rare:107 | ||||
| chr16:53576-53895 | Common:7; Rare:107 | ||||
| chr16:78131-78285 | Common:3; Rare:57 | ||||
| chr16:398163-398194 | Common:1; Rare:13 | ||||
| chr16:401716-401964 | Common:2; Rare:106 | ||||
| chr16:641744-641960 | Common:3; Rare:75 | ||||
| chr16:679765-680142 | Common:8; Rare:101 | ||||
| chr16:680377-680577 | Common:1; Rare:64 | ||||
| chr16:684112-684473 | Common:2; Rare:177 | ||||
| chr16:721096-721203 | Common:3; Rare:30 | ||||
| chr16:726879-727149 | Common:5; Rare:69 | ||||
| chr16:1351852-1351965 | Common:1; Rare:52; Clinvar:3; Clinvar (benign):1 |