| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89720264-89720456 | Common:3; Rare:50 | ||||
| chr16:89720545-89720653 | Common:2; Rare:29 | ||||
| chr16:89720835-89721111 | Common:2; Rare:83 | ||||
| chr16:89721371-89721646 | Common:3; Rare:124 | ||||
| chr16:89721649-89721976 | Rare:111 | ||||
| chr16:89765035-89765162 | Common:3; Rare:61; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr16:89816071-89816188 | Common:1; Rare:57 | ||||
| chr16:89816448-89816977 | Common:9; Rare:261; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):5 | ||||
| chr16:89816978-89817063 | Rare:51 | ||||
| chr16:89817065-89817082 | Rare:6 | ||||
| chr16:89828233-89828578 | Common:3; Rare:134 | ||||
| chr16:89828909-89829104 | Common:1; Rare:58 | ||||
| chr16:89872955-89873217 | Common:3; Rare:73 | ||||
| chr16:89873336-89873705 | Common:5; Rare:158 | ||||
| chr16:89873823-89873953 | Common:3; Rare:41 |