| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:21952983-21953445 | Common:1; Rare:116; Clinvar (benign):3 | ||||
| chr16:22206014-22206335 | Common:1; Rare:85 | ||||
| chr16:22436939-22437071 | Rare:51 | ||||
| chr16:22437142-22437313 | Rare:53 | ||||
| chr16:22437500-22437716 | Common:2; Rare:55 | ||||
| chr16:23452709-23452817 | Rare:40; Clinvar (benign):1 | ||||
| chr16:23557294-23557652 | Common:3; Rare:128; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23641212-23641551 | Common:2; Rare:98; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23678681-23678942 | Common:5; Rare:80 | ||||
| chr16:24539348-24539612 | Common:1; Rare:92 | ||||
| chr16:24540241-24540473 | Rare:63 | ||||
| chr16:24729607-24729739 | Common:6; Rare:70 | ||||
| chr16:25015329-25015420 | Rare:37 | ||||
| chr16:25111468-25111796 | Common:2; Rare:84 | ||||
| chr16:27268713-27268891 | Common:1; Rare:67 |