| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:21278247-21278399 | Common:2; Rare:32 | ||||
| chr16:21283607-21283904 | Common:4; Rare:83 | ||||
| chr16:21599364-21599742 | Common:4; Rare:130 | ||||
| chr16:21704773-21704986 | Common:2; Rare:48 | ||||
| chr16:21952959-21953455 | Common:1; Rare:126; Clinvar (benign):3 | ||||
| chr16:22001073-22001214 | Rare:36 | ||||
| chr16:22092245-22092541 | Rare:49 | ||||
| chr16:22373990-22374028 | Rare:12 | ||||
| chr16:22374593-22374883 | Common:1; Rare:96 | ||||
| chr16:22436702-22436713 | Rare:2 | ||||
| chr16:22436919-22437491 | Rare:194 | ||||
| chr16:22437513-22437695 | Common:2; Rare:46 | ||||
| chr16:23452680-23452794 | Rare:37 | ||||
| chr16:23453159-23453262 | Rare:30 | ||||
| chr16:23557278-23557475 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):4 |