| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3400975-3401248 | Common:6; Rare:98 | ||||
| chr16:4425750-4425879 | Common:1; Rare:61 | ||||
| chr16:4476273-4476459 | Common:3; Rare:68 | ||||
| chr16:4538400-4538611 | Common:1; Rare:73 | ||||
| chr16:5097740-5098014 | Common:4; Rare:96 | ||||
| chr16:8797621-8797866 | Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:8868975-8869244 | Common:4; Rare:121 | ||||
| chr16:11345292-11345451 | Common:1; Rare:53 | ||||
| chr16:11586891-11587036 | Common:1; Rare:44 | ||||
| chr16:11915900-11916208 | Common:2; Rare:124 | ||||
| chr16:15094254-15094478 | Rare:107 | ||||
| chr16:18801468-18801871 | Common:4; Rare:140 | ||||
| chr16:20806432-20806530 | Rare:40 | ||||
| chr16:21953012-21953413 | Common:1; Rare:100; Clinvar (benign):3 | ||||
| chr16:23557336-23557562 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):1 |