| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69132537-69132680 | Rare:60 | ||||
| chr16:69339548-69339807 | Rare:102; Clinvar (benign):1 | ||||
| chr16:69726537-69726804 | Common:3; Rare:62 | ||||
| chr16:70114127-70114376 | Common:3; Rare:89 | ||||
| chr16:70299154-70299233 | Rare:20 | ||||
| chr16:70346810-70346965 | Common:1; Rare:78 | ||||
| chr16:70523527-70523836 | Common:3; Rare:100; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:71809057-71809274 | Common:3; Rare:77 | ||||
| chr16:71845895-71846017 | Common:2; Rare:39 | ||||
| chr16:71895292-71895584 | Common:3; Rare:109 | ||||
| chr16:72093579-72093934 | Rare:89 | ||||
| chr16:74296462-74296920 | Common:1; Rare:153 | ||||
| chr16:75433399-75433812 | Common:4; Rare:123 | ||||
| chr16:75647614-75647803 | Common:2; Rare:96; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648084-75648343 | Rare:98 |