| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70346751-70346965 | Common:1; Rare:107 | ||||
| chr16:70523530-70523861 | Common:3; Rare:107; Clinvar (pathogenic):1 | ||||
| chr16:71808772-71808871 | Common:1; Rare:53 | ||||
| chr16:71895330-71895574 | Rare:84 | ||||
| chr16:72008514-72008772 | Common:5; Rare:95; Clinvar (benign):1 | ||||
| chr16:72093598-72093957 | Rare:86 | ||||
| chr16:74296676-74296902 | Rare:94 | ||||
| chr16:74607070-74607206 | Rare:72 | ||||
| chr16:74666889-74667166 | Common:4; Rare:88 | ||||
| chr16:75433359-75433812 | Common:4; Rare:146 | ||||
| chr16:75623229-75623435 | Common:3; Rare:73 | ||||
| chr16:75647624-75647809 | Common:2; Rare:92; Clinvar:4 | ||||
| chr16:81006825-81007282 | Common:3; Rare:154 | ||||
| chr16:82626866-82627042 | Rare:45 | ||||
| chr16:84116770-84117087 | Common:4; Rare:130 |