| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:18926312-18926605 | Common:3; Rare:127 | ||||
| chr16:19067773-19067932 | Common:2; Rare:39 | ||||
| chr16:19113818-19113974 | Common:1; Rare:32 | ||||
| chr16:20763925-20764057 | Common:2; Rare:21 | ||||
| chr16:20806337-20806484 | Rare:52 | ||||
| chr16:20900226-20900892 | Common:4; Rare:156 | ||||
| chr16:21158443-21158735 | Common:2; Rare:80 | ||||
| chr16:21952991-21953413 | Common:1; Rare:108; Clinvar (benign):3 | ||||
| chr16:22436942-22437129 | Rare:68 | ||||
| chr16:22437166-22437320 | Rare:46 | ||||
| chr16:22437345-22437667 | Common:2; Rare:91 | ||||
| chr16:22814774-22815010 | Common:1; Rare:79 | ||||
| chr16:23557327-23557557 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641247-23641533 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:24540303-24540454 | Rare:42 |