| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88706321-88706584 | Common:9; Rare:243 | ||||
| chr16:88785143-88785311 | Common:2; Rare:65 | ||||
| chr16:88785460-88785730 | Rare:80 | ||||
| chr16:88803592-88803842 | Common:9; Rare:212 | ||||
| chr16:88811857-88812096 | Common:4; Rare:169; Clinvar (benign):2 | ||||
| chr16:88856869-88857171 | Common:8; Rare:249; Clinvar:3; Clinvar (benign):4 | ||||
| chr16:89093769-89093964 | Common:3; Rare:83 | ||||
| chr16:89199990-89200250 | Common:1; Rare:127 | ||||
| chr16:89200301-89200444 | Rare:73 | ||||
| chr16:89200460-89200830 | Common:3; Rare:97 | ||||
| chr16:89201597-89201997 | Common:6; Rare:262 | ||||
| chr16:89217591-89217776 | Common:2; Rare:167 | ||||
| chr16:89490476-89490980 | Common:12; Rare:353 | ||||
| chr16:89507710-89508170 | Common:4; Rare:174 | ||||
| chr16:89508230-89508445 | Common:3; Rare:210; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 |