| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1782418-1782892 | Common:8; Rare:261 | ||||
| chr16:1782812-1783018 | Rare:68 | ||||
| chr16:1826532-1827010 | Common:13; Rare:243 | ||||
| chr16:1827124-1827590 | Common:6; Rare:388 | ||||
| chr16:1943142-1943519 | Common:2; Rare:238 | ||||
| chr16:1959373-1959655 | Common:11; Rare:211 | ||||
| chr16:1964588-1965074 | Common:23; Rare:333 | ||||
| chr16:1971867-1972148 | Common:6; Rare:161 | ||||
| chr16:1983951-1984234 | Common:5; Rare:89; Clinvar (benign):3 | ||||
| chr16:1984447-1984790 | Common:2; Rare:173; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:2009703-2009978 | Common:25; Rare:196 | ||||
| chr16:2026783-2026920 | Common:1; Rare:50 | ||||
| chr16:2035500-2036150 | Common:5; Rare:211 | ||||
| chr16:2047080-2047450 | Common:3; Rare:181 | ||||
| chr16:2047723-2048049 | Rare:292; Clinvar:4; Clinvar (benign):2 |