| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:15888587-15888811 | Common:2; Rare:81 | ||||
| chr16:18790256-18790457 | Common:4; Rare:75 | ||||
| chr16:18926399-18926629 | Common:2; Rare:93 | ||||
| chr16:19067401-19067702 | Common:5; Rare:118; Clinvar:1 | ||||
| chr16:19067773-19067925 | Common:2; Rare:39 | ||||
| chr16:19113827-19113967 | Rare:27 | ||||
| chr16:20676154-20676245 | Common:2; Rare:18 | ||||
| chr16:20806337-20806527 | Rare:68 | ||||
| chr16:20900308-20900892 | Common:4; Rare:137 | ||||
| chr16:21303018-21303232 | Rare:43 | ||||
| chr16:21952975-21953425 | Common:1; Rare:112; Clinvar (benign):3 | ||||
| chr16:22437110-22437313 | Rare:68 | ||||
| chr16:22437513-22437685 | Common:2; Rare:42 | ||||
| chr16:23557325-23557551 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23641234-23641551 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):3 |