| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89560488-89560963 | Rare:346 | ||||
| chr16:89620410-89620767 | Rare:194 | ||||
| chr16:89657634-89658111 | Common:6; Rare:494 | ||||
| chr16:89687286-89687519 | Rare:128 | ||||
| chr16:89701627-89701839 | Common:2; Rare:148 | ||||
| chr16:89701930-89702250 | Common:9; Rare:99 | ||||
| chr16:89711597-89711896 | Common:6; Rare:217 | ||||
| chr16:89720410-89720810 | Common:6; Rare:234 | ||||
| chr16:89720862-89721068 | Common:2; Rare:114 | ||||
| chr16:89721270-89721635 | Common:6; Rare:228 | ||||
| chr16:89816502-89816945 | Common:15; Rare:359; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):8 | ||||
| chr16:89817450-89817940 | Common:4; Rare:193 | ||||
| chr16:89828182-89828559 | Common:5; Rare:275 | ||||
| chr16:89873428-89873794 | Common:7; Rare:302 | ||||
| chr16:89873769-89873987 | Common:5; Rare:83 |