| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:100423991-100424307 | Common:1; Rare:67 | ||||
| chr15:100431111-100431308 | Common:1; Rare:30 | ||||
| chr15:101961584-101961633 | |||||
| chr16:83567-83704 | Common:3; Rare:32 | ||||
| chr16:264653-264858 | Common:2; Rare:91 | ||||
| chr16:528822-529187 | Common:2; Rare:96 | ||||
| chr16:619848-619970 | Common:2; Rare:31 | ||||
| chr16:1200640-1200806 | Common:2; Rare:92; Clinvar:2; Clinvar (benign):4 | ||||
| chr16:1203848-1203865 | Rare:7 | ||||
| chr16:1204651-1204961 | Common:8; Rare:66 | ||||
| chr16:1206800-1207427 | Common:5; Rare:276; Clinvar:3; Clinvar (benign):4 | ||||
| chr16:1210676-1210897 | Common:1; Rare:112; Clinvar:6; Clinvar (benign):5 | ||||
| chr16:1213078-1213260 | Common:2; Rare:65 | ||||
| chr16:1213734-1213803 | Rare:33; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:1216322-1216518 | Common:4; Rare:60 |