| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1351832-1352003 | Common:2; Rare:92; Clinvar:6; Clinvar (benign):1 | ||||
| chr16:1420687-1420937 | Common:1; Rare:108 | ||||
| chr16:1474990-1475116 | Common:3; Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:1493271-1493602 | Common:4; Rare:100 | ||||
| chr16:1706026-1706272 | Common:2; Rare:79 | ||||
| chr16:1771499-1771862 | Common:3; Rare:143 | ||||
| chr16:1773062-1773235 | Rare:62; Clinvar (pathogenic):1 | ||||
| chr16:1782507-1782772 | Common:4; Rare:85 | ||||
| chr16:1782775-1783032 | Rare:92 | ||||
| chr16:1826783-1826948 | Common:2; Rare:50 | ||||
| chr16:1827157-1827255 | Common:1; Rare:50 | ||||
| chr16:1943106-1943508 | Common:1; Rare:126 | ||||
| chr16:1959478-1959751 | Common:4; Rare:126 | ||||
| chr16:1964275-1964583 | Common:5; Rare:127 | ||||
| chr16:1964588-1965061 | Common:16; Rare:218 |