| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1826780-1827010 | Common:5; Rare:78 | ||||
| chr16:1827135-1827530 | Common:3; Rare:197 | ||||
| chr16:1943111-1943513 | Common:1; Rare:129 | ||||
| chr16:1959468-1959750 | Common:4; Rare:127 | ||||
| chr16:1964804-1965074 | Common:7; Rare:120 | ||||
| chr16:1971927-1972123 | Common:1; Rare:56 | ||||
| chr16:1975041-1975216 | Common:2; Rare:77 | ||||
| chr16:2009645-2009926 | Common:15; Rare:115 | ||||
| chr16:2047795-2048050 | Rare:121; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2155491-2155820 | Common:1; Rare:96 | ||||
| chr16:2205683-2205896 | Common:4; Rare:99 | ||||
| chr16:2223304-2223636 | Rare:132 | ||||
| chr16:2268053-2268182 | Common:1; Rare:68 | ||||
| chr16:2268351-2268497 | Common:1; Rare:53 | ||||
| chr16:2429146-2429484 | Common:3; Rare:111 |