| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70346797-70346947 | Common:1; Rare:74 | ||||
| chr16:70454540-70454620 | Rare:17 | ||||
| chr16:70523527-70523855 | Common:3; Rare:108; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:71289375-71289658 | Common:2; Rare:96 | ||||
| chr16:71808766-71808869 | Common:1; Rare:56 | ||||
| chr16:71809048-71809308 | Common:3; Rare:88 | ||||
| chr16:71845895-71846017 | Common:2; Rare:39 | ||||
| chr16:71895379-71895574 | Rare:67 | ||||
| chr16:72093579-72094017 | Common:1; Rare:107 | ||||
| chr16:74296719-74296920 | Rare:85 | ||||
| chr16:74607082-74607200 | Rare:60 | ||||
| chr16:74701119-74701344 | Common:1; Rare:47 | ||||
| chr16:75433402-75433798 | Common:4; Rare:120 | ||||
| chr16:75623232-75623368 | Common:3; Rare:46 | ||||
| chr16:75647635-75647809 | Common:2; Rare:82; Clinvar:3 |