| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2268080-2268178 | Common:1; Rare:43 | ||||
| chr16:2752587-2752680 | Rare:33 | ||||
| chr16:2777244-2777413 | Common:3; Rare:67 | ||||
| chr16:3134821-3135141 | Common:3; Rare:86 | ||||
| chr16:3305476-3305514 | Rare:11 | ||||
| chr16:3400996-3401193 | Common:3; Rare:74 | ||||
| chr16:4847273-4847516 | Common:3; Rare:116 | ||||
| chr16:5033928-5033958 | Rare:8 | ||||
| chr16:8797621-8797879 | Rare:101; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:11797136-11797543 | Common:4; Rare:154 | ||||
| chr16:11976618-11976758 | Common:2; Rare:49 | ||||
| chr16:23641278-23641518 | Common:2; Rare:66; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:25111556-25111762 | Common:1; Rare:46 | ||||
| chr16:27549886-27550161 | Common:2; Rare:98 | ||||
| chr16:28846296-28846606 | Common:2; Rare:107; Clinvar:5; Clinvar (benign):3 |