| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1063665-1064065 | Common:15; Rare:186 | ||||
| chr16:1296830-1297180 | Common:1; Rare:70 | ||||
| chr16:1304329-1304515 | Common:2; Rare:46 | ||||
| chr16:1310307-1310525 | Common:1; Rare:65 | ||||
| chr16:1331780-1332090 | Common:6; Rare:164 | ||||
| chr16:1361560-1362425 | Common:4; Rare:631; Clinvar:16; Clinvar (benign):7; Clinvar (pathogenic):17 | ||||
| chr16:1408139-1408440 | Common:12; Rare:223 | ||||
| chr16:1469430-1469940 | Common:7; Rare:146 | ||||
| chr16:1469932-1470090 | Common:1; Rare:30 | ||||
| chr16:1471074-1471190 | Common:1; Rare:26 | ||||
| chr16:1482290-1482690 | Common:10; Rare:183 | ||||
| chr16:1543520-1543820 | Common:2; Rare:81 | ||||
| chr16:1545290-1545620 | Common:2; Rare:58 | ||||
| chr16:1596856-1597518 | Common:6; Rare:272 | ||||
| chr16:1620331-1620787 | Common:3; Rare:209 |