| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:83011577-83011770 | Common:2; Rare:78 | ||||
| chr15:88467332-88467749 | Common:5; Rare:137 | ||||
| chr15:90233905-90234256 | Common:6; Rare:97 | ||||
| chr15:91022590-91022606 | Rare:3 | ||||
| chr15:101295197-101295409 | Common:1; Rare:67 | ||||
| chr16:138652-138784 | Common:3; Rare:41 | ||||
| chr16:636274-636427 | Common:4; Rare:52 | ||||
| chr16:680295-680506 | Common:2; Rare:71 | ||||
| chr16:721066-721191 | Common:3; Rare:36 | ||||
| chr16:1351830-1351960 | Common:2; Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:1773126-1773216 | Rare:22 | ||||
| chr16:1782510-1783009 | Common:4; Rare:165 | ||||
| chr16:1826785-1826938 | Common:1; Rare:44 | ||||
| chr16:1964824-1965059 | Common:6; Rare:100 | ||||
| chr16:2047724-2048045 | Rare:157; Clinvar:2; Clinvar (benign):1 |